
[Federal Register Volume 78, Number 187 (Thursday, September 26, 2013)]
[Notices]
[Pages 59347-59359]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2013-23368]


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ENVIRONMENTAL PROTECTION AGENCY

[EPA-HQ-OPP-2013-0621; FRL-9399-5]


Pesticides; Revised Fee Schedule for Registration Applications

AGENCY: Environmental Protection Agency (EPA).

ACTION: Notice.

-----------------------------------------------------------------------

SUMMARY: EPA is publishing a revised list of pesticide registration 
service fees applicable to specified pesticide applications and 
tolerance actions. Under the Pesticide Registration Improvement 
Extension Act, the registration service fees for covered pesticide 
registration applications received on or after October 1, 2013, 
increase by 5% rounding up to the nearest dollar from the fees 
published for fiscal year 2012. The new fees become effective on 
October 1, 2013.

FOR FURTHER INFORMATION CONTACT: Peter Caulkins (7501P), Immediate 
Office, Office of Pesticide Programs, Environmental Protection Agency, 
1200 Pennsylvania Ave. NW., Washington, DC 20460-0001; telephone 
number: (703) 305-6550; fax number: (703) 308-4776; email address: 
caulkins.peter@epa.gov.

SUPPLEMENTARY INFORMATION:

I. General Information

A. Does this action apply to me?

    You may be potentially affected by this action if you register 
pesticide products under the Federal Insecticide, Fungicide, and 
Rodenticide Act (FIFRA). Potentially affected entities may include, but 
are not limited to:
     Agricultural pesticide manufacturers (NAICS code 32532).
     Antimicrobial pesticide manufacturers (NAICS code 32561).
     Antifoulant pesticide manufacturers (NAICS code 32551).
     Wood preservative manufacturers (NAICS code 32519).
    This listing is not intended to be exhaustive, but rather provides 
a guide for readers regarding entities likely to be affected by this 
action. Other types of entities not listed in this unit could also be 
affected. The North American

[[Page 59348]]

Industrial Classification System (NAICS) codes have been provided to 
assist you and others in determining whether this action might apply to 
certain entities. To determine whether you or your business may be 
affected by this action, you should carefully examine the applicability 
provisions in the notice and in FIFRA section 33. If you have any 
questions regarding the applicability of this action to a particular 
entity, consult the person listed under FOR FURTHER INFORMATION 
CONTACT.

B. How can I get copies of this document and other related information?

    The docket for this action, identified by docket identification 
(ID) number EPA-HQ-OPP-2013-0621, is available at http://www.regulations.gov or at the Office of Pesticide Programs Regulatory 
Public Docket (OPP Docket) in the Environmental Protection Agency 
Docket Center (EPA/DC), EPA West Bldg., Rm. 3334, 1301 Constitution 
Ave. NW., Washington, DC 20460-0001. The Public Reading Room is open 
from 8:30 a.m. to 4:30 p.m., Monday through Friday, excluding legal 
holidays. The telephone number for the Public Reading Room is (202) 
566-1744, and the telephone number for the OPP Docket is (703) 305-
5805. Please review the visitor instructions and additional information 
about the docket available at http://www.epa.gov/dockets.

II. Background

A. What action is the Agency taking?

    The Pesticide Registration Improvement Act of 2003 established a 
new section 33 of FIFRA creating a registration service fee system for 
certain types of pesticide applications, establishment of tolerances, 
and certain other regulatory decisions under FIFRA and the Federal 
Food, Drug, and Cosmetic Act (FFDCA). Section 33 also created a 
schedule of decision review times for applications covered by the 
service fee system. The Agency began administering the registration 
service fee system for covered applications received on or after March 
23, 2004.
    On September 28, 2012, the Pesticide Registration Improvement 
Extension Act was signed by the President, revising, among other 
things, FIFRA section 33. The new law reauthorized the service fee 
system through fiscal year 2017 and established fees and review times 
for applications received during fiscal years 2013 through 2017. As 
required by section 33(b)(6)(A) of FIFRA, the registration service fees 
for covered pesticide registration applications received on or after 
October 1, 2013, increase by 5% rounding up to the nearest dollar from 
the fees published in the September 28, 2012 Pesticide Registration 
Improvement Extension Act.

B. What is the Agency's authority for taking this action?

    The publication of this fee schedule is required by section 
33(b)(6)(C) of FIFRA as amended.

III. Elements of the Fee Schedule

    This unit explains how to read the fee schedule tables, and 
includes a key to terminology published with the table.

A. The Pesticide Registration Improvement Extension Act Fee Schedule

    The fee schedule published in the Pesticide Registration 
Improvement Extension Act of September 28, 2013, identifies the 
registration service fees and decision times and is organized according 
to the organizational units of the Office of Pesticide Programs (OPP) 
within EPA. Thereafter, the categories within the organizational unit 
sections of the table are further categorized according to the type of 
application being submitted, the use patterns involved, or, in some 
cases, upon the type of pesticide that is the subject of the 
application. The fee categories differ by Division. Not all application 
types are covered by, or subject to, the fee system.

B. Fee Schedule and Decision Review Times

    In today's notice, EPA has retained the format of the tables 
included in the Pesticide Registration Improvement Extension Act of 
September 28, 2012. The schedules are presented as 18 tables, organized 
by OPP Division and by type of application or pesticide subject to the 
fee. Unit IV. presents fee tables for the Registration Division (RD) (6 
tables), the Antimicrobials Division (AD) (4 tables), the Biopesticides 
and Pollution Prevention Division (BPPD) (7 tables), and Inert 
Ingredients, External Review and Miscellaneous (1 table).

C. How To Read the Tables

1. Each table consists of the following columns:
     The column titled ``EPA No.''' assigns an EPA identifier 
to each fee category. There are 189 categories spread across the 3 
Divisions. There are 63 RD categories, 39 AD categories, 69 BPPD 
categories, 10 inert categories, and 8 miscellaneous categories. For 
tracking purposes, OPP has assigned a 3-digit identifier to each 
category, beginning with RD categories, followed by AD, BPPD, inert and 
miscellaneous categories. The categories are prefaced with a letter 
designation indicating which Division of OPP is responsible for 
applications in that category (R=Registration Division, 
A=Antimicrobials Division, B=Biopesticides and Pollution Prevention 
Division, I=inert ingredients, M= miscellaneous).
     The column titled ``CR No.'' cross-references the current 
Congressional Record category number for convenience. However, EPA will 
be using the categories as numbered in the ``EPA No.'' column in its 
tracking systems.
     The column titled ``Action''' describes what registration 
actions are covered by each category.
     The column titled ``Decision Time'' lists the decision 
times in months for each type of action.
     The column titled ``FY 2014/FY 2015 Registration Service 
Fee ($)'' lists the registration service fee for the action for fiscal 
year 2014 (October 1, 2013 through September 30, 2014) and fiscal year 
2015 (October 1, 2014 through September 30, 2015).
     Footnote text has been removed to save on Federal Register 
costs but remains unchanged from what was published in FY 2013. The 
tables and footnote text will be available in full after October 1 at 
http://www.epa.gov/pesticides/regulating/fees/tool/category-table.html.
2. The following acronyms are used in some of the tables:
     DART-Dose Adequacy Response Team.
     DNT-Developmental Neurotoxicity.
     HSRB-Human Studies Review Board.
     GW/SW-Ground Water/Surface Water.
     PHI-Pre-Harvest Interval.
     PPE-Personal Protective Equipment.
     REI-Restricted Entry Interval.
     SAP-FIFRA Scientific Advisory Panel.

IV. PRIA Fee Schedule Tables--Effective October 1, 2013

A. Registration Division (RD)

    The Registration Division of OPP is responsible for the processing 
of pesticide applications and associated tolerance petitions for 
pesticides that are termed ``conventional chemicals,'' excluding 
pesticides intended for antimicrobial uses. The term ``conventional 
chemical'' is a term of art that is intended to distinguish synthetic 
chemicals from those that are of naturally occurring or non-synthetic

[[Page 59349]]

origin, synthetic chemicals that are identical to naturally occurring 
chemicals and microbial pesticides. Tables 1 through 6 cover RD 
actions.

                             Table 1--Registration Division--New Active Ingredients
----------------------------------------------------------------------------------------------------------------
                                                                                                     FY '14/15
                                                                                     Decision      registration
           EPA No.               New CR No.                  Action                 review time     service fee
                                                                                     (months)           ($)
----------------------------------------------------------------------------------------------------------------
R010.........................               1  New active ingredient, food use..              24         597,683
R020.........................               2  New active ingredient, food use;               18         597,683
                                                reduced risk.
R040.........................               3  New active ingredient, food use;               18         440,478
                                                Experimental Use Permit
                                                application; establish temporary
                                                tolerance; submitted before
                                                application for registration;
                                                credit 45% of fee toward new
                                                active ingredient application
                                                that follows.
R060.........................               4  New active ingredient, non-food                21         415,241
                                                use; outdoor.
R070.........................               5  New active ingredient, non-food                16         415,241
                                                use; outdoor; reduced risk.
R090.........................               6  New active ingredient, non-food                16         308,276
                                                use; outdoor; Experimental Use
                                                Permit application; submitted
                                                before application for
                                                registration; credit 45% of fee
                                                toward new active ingredient
                                                application that follows.
R110.........................               7  New active ingredient, non-food                20         230,947
                                                use; indoor.
R120.........................               8  New active ingredient, non-food                14         230,947
                                                use; indoor; reduced risk.
R121.........................               9  New active ingredient, non-food                18         173,644
                                                use; indoor; Experimental Use
                                                Permit application; submitted
                                                before application for
                                                registration; credit 45% of fee
                                                toward new active ingredient
                                                application that follows.
R122.........................              10  Enriched isomer(s) of registered               18         302,026
                                                mixed-isomer active ingredient.
R123.........................              11  New active ingredient, seed                    18         449,391
                                                treatment only; includes
                                                agricultural and non-
                                                agricultural seeds; residues not
                                                expected in raw agricultural
                                                commodities.
R125.........................              12  New active ingredient, seed                    16         308,276
                                                treatment; Experimental Use
                                                Permit application; submitted
                                                before application for
                                                registration; credit 45% of fee
                                                toward new active ingredient
                                                application that follows.
----------------------------------------------------------------------------------------------------------------


                                    Table 2--Registration Division--New Uses
----------------------------------------------------------------------------------------------------------------
                                                                                                     FY '14/15
                                                                                     Decision      registration
           EPA No.               New CR No.                  Action                 review time     service fee
                                                                                     (months)           ($)
----------------------------------------------------------------------------------------------------------------
R130.........................              13  First food use; indoor; food/food              21         182,327
                                                handling.
R140.........................              14  Additional food use; indoor; food/             15          42,544
                                                food handling.
R150.........................              15  First food use...................              21         251,669
R160.........................              16  First food use; reduced risk.....              16         251,669
R170.........................              17  Additional food use..............              15          62,975
R175.........................              18  Additional food uses covered                   10          62,975
                                                within a crop group resulting
                                                from the conversion of existing
                                                approved crop group(s) to one or
                                                more revised crop groups.
R180.........................              19  Additional food use; reduced risk              10          62,975
R190.........................              20  Additional food uses; six or more              15         377,849
                                                submitted in one application.
R200.........................              21  Additional food use; six or more               10         377,849
                                                submitted in one application;
                                                reduced risk.
R210.........................              22  Additional food use; Experimental              12          46,653
                                                Use Permit application;
                                                establish temporary tolerance;
                                                no credit toward new use
                                                registration.
R220.........................              23  Additional food use; Experimental               6          18,893
                                                Use Permit application; crop
                                                destruct basis; no credit toward
                                                new use registration.
R230.........................              24  Additional use; non-food; outdoor              15          25,168
R240.........................              25  Additional use; non-food;                      10          25,168
                                                outdoor; reduced risk.
R250.........................              26  Additional use; non-food;                       6          18,893
                                                outdoor; Experimental Use Permit
                                                application; no credit toward
                                                new use registration.
R251.........................              27  Experimental Use Permit                         8          18,893
                                                application which requires no
                                                changes to the tolerance(s); non-
                                                crop destruct basis.
R260.........................              28  New use; non-food; indoor........              12          12,156
R270.........................              29  New use; non-food; indoor;                      9          12,156
                                                reduced risk.
R271.........................              30  New use; non-food; indoor;                      6           9,261
                                                Experimental Use Permit
                                                application; no credit toward
                                                new use registration.
R273.........................              31  Additional use; seed treatment;                12          48,042
                                                limited uptake into raw
                                                agricultural commodities;
                                                includes crops with established
                                                tolerances (e.g., for soil or
                                                foliar application); includes
                                                food and/or non-food uses.
R274.........................              32  Additional uses; seed treatment                12         288,250
                                                only; six or more submitted in
                                                one application; limited uptake
                                                into raw agricultural
                                                commodities; includes crops with
                                                established tolerances (e.g.,
                                                for soil or foliar application);
                                                includes food and/or non-food
                                                uses.
----------------------------------------------------------------------------------------------------------------


[[Page 59350]]


                           Table 3--Registation Division--Import and Other Tolerances
----------------------------------------------------------------------------------------------------------------
                                                                                                     FY '14/15
                                                                                     Decision      registration
           EPA No.               New CR No.                  Action                 review time     service fee
                                                                                     (months)           ($)
----------------------------------------------------------------------------------------------------------------
R280.........................              33  Establish import tolerance; new                21         303,878
                                                active ingredient or first food
                                                use.
R290.........................              34  Establish Import tolerance;                    15          60,777
                                                additional new food use.
R291.........................              35  Establish import tolerances;                   15         364,653
                                                additional food uses; six or
                                                more crops submitted in one
                                                petition.
R292.........................              36  Amend an established tolerance                 11          43,181
                                                (e.g., decrease or increase);
                                                domestic or import; applicant-
                                                initiated.
R293.........................              37  Establish tolerance(s) for                     12          50,936
                                                inadvertent residues in one
                                                crop; applicant-initiated.
R294.........................              38  Establish tolerances for                       12         305,613
                                                inadvertent residues; six or
                                                more crops submitted in one
                                                application; applicant-initiated.
R295.........................              39  Establish tolerance(s) for                     15          62,975
                                                residues in one rotational crop
                                                in response to a specific
                                                rotational crop application;
                                                applicant-initiated.
R296.........................              40  Establish tolerances for residues              15         377,849
                                                in rotational crops in response
                                                to a specific rotational crop
                                                petition; six or more crops
                                                submitted in one application;
                                                applicant-initiated.
R297.........................              41  Amend six or more established                  11         259,082
                                                tolerances (e.g., decrease or
                                                increase) in one petition;
                                                domestic or import; applicant-
                                                initiated.
R298.........................              42  Amend an established tolerance                 13          55,776
                                                (e.g., decrease or increase);
                                                domestic or import; submission
                                                of amended labels (requiring
                                                science review) in addition to
                                                those associated with the
                                                amended tolerance; applicant-
                                                initiated).
R299.........................              43  Amend six or more established                  13         271,677
                                                tolerances (e.g., decrease or
                                                increase); domestic or import;
                                                submission of amended labels
                                                (requiring science review) in
                                                addition to those associated
                                                with the amended tolerance;
                                                applicant-initiated).
----------------------------------------------------------------------------------------------------------------


                                  Table 4--Registration Division--New Products
----------------------------------------------------------------------------------------------------------------
                                                                                                     FY '14/15
                                                                                     Decision      registration
           EPA No.               New CR No.                  Action                 review time     service fee
                                                                                     (months)           ($)
----------------------------------------------------------------------------------------------------------------
R300.........................              44  New product; or similar                         4           1,506
                                                combination product (already
                                                registered) to an identical or
                                                substantially similar in
                                                composition and use to a
                                                registered product; registered
                                                source of active ingredient; no
                                                data review on acute toxicity,
                                                efficacy or CRP--only product
                                                chemistry data; cite-all data
                                                citation, or selective data
                                                citation where applicant owns
                                                all required data, or applicant
                                                submits specific authorization
                                                letter from data owner. Category
                                                also includes 100% repackage of
                                                registered end-use or
                                                manufacturing-use product that
                                                requires no data submission nor
                                                data matrix.
R301.........................              45  New product; or similar                         4           1,806
                                                combination product (already
                                                registered) to an identical or
                                                substantially similar in
                                                composition and use to a
                                                registered product; registered
                                                source of active ingredient;
                                                selective data citation only for
                                                data on product chemistry and/or
                                                acute toxicity and/or public
                                                health pest efficacy, where
                                                applicant does not own all
                                                required data and does not have
                                                a specific authorization letter
                                                from data owner.
R310.........................              46  New end-use or manufacturing-use                7           5,048
                                                product with registered
                                                source(s) of active
                                                ingredient(s); includes products
                                                containing two or more
                                                registered active ingredients
                                                previously combined in other
                                                registered products; requires
                                                review of data package within RD
                                                only; includes data and/or
                                                waivers of data for only:
                                                product chemistry and/or
                                                acute toxicity and/or...
                                                public health pest
                                                efficacy and/or.
                                                child resistant
                                                packaging.
R314.........................              47  New end-use product containing                  8           6,310
                                                two or more registered active
                                                ingredients never before
                                                registered as this combination
                                                in a formulated product; new
                                                product label is identical or
                                                substantially similar to the
                                                labels of currently registered
                                                products which separately
                                                contain the respective component
                                                active ingredients; requires
                                                review of data package within RD
                                                only; includes data and/or
                                                waivers of data for only:
                                                product chemistry and/or
                                                acute toxicity and/or...
                                                public health pest
                                                efficacy and/or.
                                                child resistant
                                                packaging.

[[Page 59351]]

 
R315.........................              48  New end-use non-food animal                     9           8,400
                                                product with submission of two
                                                or more target animal safety
                                                studies; includes data and/or
                                                waivers of data for only:
                                                product chemistry and/or
                                                acute toxicity and/or...
                                                public health pest
                                                efficacy and/or.
                                                animal safety studies
                                                and/or.
                                                child resistant
                                                packaging.
R320.........................              49  New product; new physical form;                12          12,596
                                                requires data review in science
                                                divisions.
R331.........................              50  New product; repack of identical                3           2,409
                                                registered end-use product as a
                                                manufacturing-use product; same
                                                registered uses only.
R332.........................              51  New manufacturing-use product;                 24         269,728
                                                registered active ingredient;
                                                unregistered source of active
                                                ingredient; submission of
                                                completely new generic data
                                                package; registered uses only;
                                                requires review in RD and
                                                science divisions.
R333.........................              52  New product; MUP or end-use                    10          18,893
                                                product with unregistered source
                                                of active ingredient; requires
                                                science data review; new
                                                physical form; etc. Cite-all or
                                                selective data citation where
                                                applicant owns all required data.
R334.........................              53  New product; MUP or end-use                    11          18,893
                                                product with unregistered source
                                                of the active ingredient;
                                                requires science data review;
                                                new physical form; etc.
                                                Selective data citation.
----------------------------------------------------------------------------------------------------------------


                           Table 5--Registration Division--Amendments to Registration
----------------------------------------------------------------------------------------------------------------
                                                                                                     FY '14/15
                                                                                     Decision      registration
           EPA No.               New CR No.                  Action                 review time     service fee
                                                                                     (months)           ($)
----------------------------------------------------------------------------------------------------------------
R340.........................              54  Amendment requiring data review                 4           3,798
                                                within RD (e.g., changes to
                                                precautionary label statements).
R345.........................              55  Amending non-food animal product                7           8,400
                                                that includes submission of
                                                target animal safety data;
                                                previously registered.
R350.........................              56  Amendment requiring data review                 9          12,596
                                                in science divisions (e.g.,
                                                changes to REI, or PPE, or PHI,
                                                or use rate, or number of
                                                applications; or add aerial
                                                application; or modify GW/SW
                                                advisory statement).
R351.........................              57  Amendment adding a new                          8          12,596
                                                unregistered source of active
                                                ingredient.
R352.........................              58  Amendment adding already approved               8          12,596
                                                uses; selective method of
                                                support; does not apply if the
                                                applicant owns all cited data.
R371.........................              59  Amendment to Experimental Use                   6           9,609
                                                Permit; (does not include
                                                extending a permit's time
                                                period).
----------------------------------------------------------------------------------------------------------------


                                  Table 6--Registration Division--Other Actions
----------------------------------------------------------------------------------------------------------------
                                                                                                     FY '14/15
                                                                                     Decision      registration
           EPA No.               New CR No.                  Action                 review time     service fee
                                                                                     (months)           ($)
----------------------------------------------------------------------------------------------------------------
R124                                       60  Conditional ruling on pre-                      6           2,409
                                                application study waivers;
                                                applicant-initiated.
R272                                       61  Review of study protocol                        3           2,409
                                                applicant-initiated; excludes
                                                DART, pre-registration
                                                conference, Rapid Response
                                                review, DNT protocol review,
                                                protocol needing HSRB review.
R275                                       62  Rebuttal of agency reviewed                     3           2,409
                                                protocol, applicant-initiated.
R370                                       63  Cancer reassessment; applicant-                18         188,809
                                                initiated.
----------------------------------------------------------------------------------------------------------------

B. Antimicrobials Division (AD)

    The Antimicrobials Division of OPP is responsible for the 
processing of pesticide applications and associated tolerances for 
conventional chemicals intended for antimicrobial uses, that is, uses 
that are defined under FIFRA section 2(mm)(1)(A), including products 
for use against bacteria, protozoa, non-agricultural fungi, and 
viruses. AD is also responsible for a selected set of conventional 
chemicals intended for other uses, including most wood preservatives 
and antifoulants. Tables 7 through 10 cover AD actions.

[[Page 59352]]



                            Table 7--Antimicrobials Division--New Active Ingredients
----------------------------------------------------------------------------------------------------------------
                                                                                                     FY '14/15
                                                                                     Decision      registration
           EPA No.               New CR No.                  Action                 review time     service fee
                                                                                     (months)           ($)
----------------------------------------------------------------------------------------------------------------
A380.........................              64  New active ingredient food use,                24         109,397
                                                establish tolerance exemption.
A390.........................              65  New active ingredient food use,                24         182,327
                                                establish tolerance.
A400.........................              66  New active ingredient, non-food                18          91,165
                                                use, outdoor, FIFRA section
                                                2(mm) uses.
A410.........................              67  New active ingredient non-food                 21         182,327
                                                use, outdoor, uses other than
                                                FIFRA section 2(mm).
A420.........................              68  New active ingredient non-food                 18          60,777
                                                use, indoor, FIFRA section 2(mm)
                                                uses.
A430.........................              69  New active ingredient, non-food                20          91,165
                                                use indoor, uses other than
                                                FIFRA section 2(mm) uses.
A431.........................              70  New active ingredient, non-food                12          63,670
                                                use; indoor; low-risk; low-
                                                toxicity food-grade active
                                                ingredient(s); efficacy testing
                                                for public health claims
                                                required under GLP and following
                                                DIS/TSS or AD-approved study
                                                protocol.
----------------------------------------------------------------------------------------------------------------


                                   Table 8--Antimicrobials Division--New Uses
----------------------------------------------------------------------------------------------------------------
                                                                                                     FY '14/15
                                                                                     Decision      registration
           EPA No.               New CR No.                  Action                 review time     service fee
                                                                                     (months)           ($)
----------------------------------------------------------------------------------------------------------------
A440.........................              71  New use, first food use;                       21          30,390
                                                establish tolerance exemption.
A450.........................              72  New use, first food use;                       21          91,165
                                                establish tolerance.
A460.........................              73  New use, additional food use;                  15          12,156
                                                establish tolerance exemption.
A470.........................              74  New use, additional food use;                  15          30,390
                                                establish tolerance.
A471.........................              75  Additional food uses; establish                15         182,335
                                                tolerances; six or more
                                                submitted in one application.
A480.........................              76  New use, additional use, non-                   9          18,234
                                                food, outdoor; FIFRA section
                                                2(mm) uses.
A481.........................              77  Additional non-food outdoor uses;               9         109,400
                                                FIFRA section 2(mm) uses; six or
                                                more submitted in one
                                                application.
A490.........................              78  New use, additional use, non-                  15          30,390
                                                food, outdoor, uses other than
                                                FIFRA section 2(mm).
A491.........................              79  Additional non-food; outdoor;                  15         182,335
                                                uses other than FIFRA section
                                                2(mm); six or more submitted in
                                                one application.
A500.........................              80  New use, additional use, non-                   9          12,156
                                                food, indoor FIFRA section 2(mm)
                                                uses.
A501.........................              81  Additional non-food; indoor;                    9          72,936
                                                FIFRA section 2(mm) uses; six or
                                                more submitted in one
                                                application.
A510.........................              82  New use, additional use, non-                  12          12,156
                                                food, indoor, other than FIFRA
                                                section 2(mm).
A511.........................              83  Additional non-food; indoor; uses              12          72,936
                                                other than FIFRA section 2(mm);
                                                six or more submitted in one
                                                application.
----------------------------------------------------------------------------------------------------------------


                          Table 9--Antimicrobials Division--New Products and Amendments
----------------------------------------------------------------------------------------------------------------
                                                                                                     FY '14/15
                                                                                     Decision      registration
           EPA No.               New CR No.                  Action                 review time     service fee
                                                                                     (months)           ($)
----------------------------------------------------------------------------------------------------------------
A530.........................              84  New product, identical or                       4           1,217
                                                substantially similar in
                                                composition and use to a
                                                registered product; no data
                                                review or only product chemistry
                                                data; cite all data citation or
                                                selective data citation where
                                                applicant owns all required
                                                data; or applicant submits
                                                specific authorization letter
                                                from data owner. Category also
                                                includes 100% re-package of
                                                registered end-use or
                                                manufacturing use product that
                                                requires no data submission nor
                                                data matrix.
A531.........................              85  New product; identical or                       4           1,737
                                                substantially similar in
                                                composition and use to a
                                                registered product; registered
                                                source of active ingredient:
                                                selective data citation only for
                                                data on product chemistry and/or
                                                acute toxicity and/or public
                                                health pest efficacy, where
                                                applicant does not own all
                                                required data and does not have
                                                a specific authorization letter
                                                from data owner.
A532.........................              86  New product; identical or                       5           4,863
                                                substantially similar in
                                                composition and use to a
                                                registered product; registered
                                                active ingredient; unregistered
                                                source of active ingredient;
                                                cite-all data citation except
                                                for product chemistry; product
                                                chemistry data submitted.
A540.........................              87  New end-use product; FIFRA                      5           4,863
                                                section 2(mm) uses only.
A550.........................              88  New end-use product; uses other                 7           4,863
                                                than FIFRA section 2(mm); non-
                                                FQPA product.
A560.........................              89  New manufacturing use product;                 12          18,234
                                                registered active ingredient;
                                                selective data citation.
A570.........................              90  Label amendment requiring data                  4           3,648
                                                review.

[[Page 59353]]

 
A572.........................              91  New product or amendment                        9          12,596
                                                requiring data review for risk
                                                assessment by Science Branch
                                                (e.g., changes to REI, or PPE,
                                                or use rate).
----------------------------------------------------------------------------------------------------------------


              Table 10--Antimicrobials Division--Experimental Use Permits and Other Type of Actions
----------------------------------------------------------------------------------------------------------------
                                                                                                     FY '14/15
                                                                                     Decision      registration
           EPA No.               New CR No.                  Action                 review time     service fee
                                                                                     (months)           ($)
----------------------------------------------------------------------------------------------------------------
A520.........................              92  Experimental Use Permit                         9           6,079
                                                application.
A521.........................              93  Review of public health efficacy                3           2,363
                                                study protocol within AD, per AD
                                                Internal Guidance for the
                                                Efficacy Protocol Review
                                                Process; Code will also include
                                                review of public health efficacy
                                                study protocol and data review
                                                for devices making pesticidal
                                                claims; applicant-initiated;
                                                Tier 1.
A522.........................              94  Review of public health efficacy               12          11,577
                                                study protocol outside AD by
                                                members of AD Efficacy Protocol
                                                Review Expert Panel; Code will
                                                also include review of public
                                                health efficacy study protocol
                                                and data review for devices
                                                making pesticidal claims;
                                                applicant-initiated; Tier 2.
A524.........................              95  New active ingredient,                         18         145,862
                                                Experimental Use Permit
                                                application; Food Use Requires
                                                Tolerance. Credit 45% of fee
                                                toward new active ingredient
                                                application that follows.
A525.........................              96  New active ingredient,                         18          87,774
                                                Experimental Use Permit
                                                application; food use requires
                                                tolerance exemption. Credit 45%
                                                of fee toward new active
                                                ingredient application that
                                                follows.
A526.........................              97  New active ingredient,                         15          91,165
                                                Experimental Use Permit
                                                application; non-food, outdoor
                                                use. Credit 45% of fee toward
                                                new active ingredient
                                                application that follows.
A527.........................              98  New active ingredient,                         15          60,900
                                                Experimental Use Permit
                                                application; non-food, indoor
                                                use. Credit 45% of fee toward
                                                new active ingredient
                                                application that follows.
A528.........................              99  Experimental Use Permit                        15          21,273
                                                application, food use; requires
                                                tolerance or tolerance exemption.
A529.........................             100  Amendment to Experimental Use                   9          10,884
                                                Permit; requires data review or
                                                risk assessment.
A523.........................             101  Review of protocol other than a                 9          11,577
                                                public health efficacy study
                                                (i.e., toxicology or exposure
                                                protocols).
A571.........................             102  Science reassessment: Cancer                   18          91,165
                                                risk, refined ecological risk,
                                                and/or endangered species;
                                                applicant-initiated.
----------------------------------------------------------------------------------------------------------------

C. Biopesticides and Pollution Prevention Division (BPPD)

    The Biopesticides and Pollution Prevention Division of OPP is 
responsible for the processing of pesticide applications for 
biochemical pesticides, microbial pesticides, and plant-incorporated 
protectants (PIPs).
    The fee tables for BPPD actions are presented by type of pesticide 
rather than by type of action: Microbial and biochemical pesticides, 
straight chain lepidopteran pheromones (SCLPs), and PIPs. Within each 
table, the types of application are the same as those in other 
divisions. Tables 11 through 17 cover BPPD actions.

   Table 11--Biopesticides and Pollution Prevention Division--Microbial and Biochemical Pesticides; New Active
                                                   Ingredients
----------------------------------------------------------------------------------------------------------------
                                                                                                     FY '14/15
                                                                                     Decision      registration
           EPA No.               New CR No.                  Action                 review time     service fee
                                                                                     (months)           ($)
----------------------------------------------------------------------------------------------------------------
B580.........................             103  New active ingredient; food use;               19          48,621
                                                petition to establish a
                                                tolerance.
B590.........................             104  New active ingredient; food use;               17          30,390
                                                petition to establish a
                                                tolerance exemption.
B600.........................             105  New active ingredient; non-food                13          18,234
                                                use.
B610.........................             106  New active ingredient;                         10          12,156
                                                Experimental Use Permit
                                                application; petition to
                                                establish a temporary tolerance
                                                or temporary tolerance exemption.
B611.........................             107  New active ingredient;                         12          12,156
                                                Experimental Use Permit
                                                application; petition to
                                                establish permanent tolerance
                                                exemption.
B612.........................             108  New active ingredient; no change               10          16,714
                                                to a permanent tolerance
                                                exemption.
B613.........................             109  New active ingredient; petition                11          16,714
                                                to convert a temporary tolerance
                                                or a temporary tolerance
                                                exemption to a permanent
                                                tolerance or tolerance exemption.

[[Page 59354]]

 
B620.........................             110  New active ingredient;                          7           6,079
                                                Experimental Use Permit
                                                application; non-food use
                                                including crop destruct.
----------------------------------------------------------------------------------------------------------------


   Table 12--Biopesticides and Pollution Prevention Division--Microbial and Biochemical Pesticides; New Active
                                                   Ingredients
----------------------------------------------------------------------------------------------------------------
                                                                                                     FY '14/15
                                                                                     Decision      registration
           EPA No.               New CR No.                  Action                 review time     service fee
                                                                                     (months)           ($)
----------------------------------------------------------------------------------------------------------------
B630.........................             111  First food use; petition to                    13          12,156
                                                establish a tolerance exemption.
B631.........................             112  New food use; petition to amend                12          12,156
                                                an established tolerance.
B640.........................             113  New food use; petition to amend                19          18,234
                                                an established tolerance.
B643.........................             114  New food use; petition to amend                10          12,156
                                                tolerance exemption.
B642.........................             115  First food use; indoor; food/food              12          30,390
                                                handling.
B644.........................             116  New use, no change to an                        8          12,156
                                                established tolerance or
                                                tolerance exemption.
B650.........................             117  New use; non-food................               7           6,079
----------------------------------------------------------------------------------------------------------------


  Table 13--Biopesticides and Pollution Prevention Division--Microbial and Biochemical Pesticides; New Products
----------------------------------------------------------------------------------------------------------------
                                                                                                     FY '14/15
                                                                                     Decision      registration
           EPA No.               New CR No.                  Action                 review time     service fee
                                                                                     (months)           ($)
----------------------------------------------------------------------------------------------------------------
B652.........................             118  New product; registered source of              13          12,156
                                                active ingredient; requires
                                                petition to amend established
                                                tolerance or tolerance
                                                exemption; requires: (1)
                                                submission of product-specific
                                                data; or (2) citation of
                                                previously reviewed and accepted
                                                data; or (3) submission or
                                                citation of data generated at
                                                government expense; or (4)
                                                submission or citation of
                                                scientifically sound rationale
                                                based on publicly available
                                                literature or other relevant
                                                information that addresses the
                                                data requirement; or (5)
                                                submission of a request for a
                                                data requirement to be waived
                                                supported by a scientifically
                                                sound rationale explaining why
                                                the data requirement does not
                                                apply.
B660.........................             119  New product; registered source of               4           1,217
                                                active ingredient(s); identical
                                                or substantially similar in
                                                composition and use to a
                                                registered product; no change in
                                                an established tolerance or
                                                tolerance exemption. No data
                                                review, or only product
                                                chemistry data; cite-all data
                                                citation, or selective data
                                                citation where applicant owns
                                                all required data or
                                                authorization from data owner is
                                                demonstrated. Category includes
                                                100% re-package of registered
                                                end-use or manufacturing-use
                                                product that requires no data
                                                submission or data matrix. For
                                                microbial pesticides, the active
                                                ingredient(s) must not be re-
                                                isolated.
B670.........................             120  New product; registered source of               7           4,863
                                                active ingredient(s); no change
                                                in an established tolerance or
                                                tolerance exemption; requires:
                                                (1) submission of product-
                                                specific data; or (2) citation
                                                of previously reviewed and
                                                accepted data; or (3) submission
                                                or citation of data generated at
                                                government expense; or (4)
                                                submission or citation of a
                                                scientifically sound rationale
                                                based on publicly available
                                                literature or other relevant
                                                information that addresses the
                                                data requirement; or (5)
                                                submission of a request for a
                                                data requirement to be waived
                                                supported by a scientifically
                                                sound rationale explaining why
                                                the data requirement does not
                                                apply.
B671.........................             121  New product; unregistered source               17          12,156
                                                of active ingredient(s);
                                                requires a petition to amend an
                                                established tolerance or
                                                tolerance exemption; requires:
                                                (1) Submission of product-
                                                specific data; or (2) citation
                                                of previously reviewed and
                                                accepted data; or (3) submission
                                                or citation of data generated at
                                                government expense; or (4)
                                                submission or citation of a
                                                scientifically sound rationale
                                                based on publicly available
                                                literature or other relevant
                                                information that addresses the
                                                data requirement; or (5)
                                                submission of a request for a
                                                data requirement to be waived
                                                supported by a scientifically
                                                sound rationale explaining why
                                                the data requirement does not
                                                apply.

[[Page 59355]]

 
B672.........................             122  New product; unregistered source               13           8,683
                                                of active ingredient(s); non-
                                                food use or food use with a
                                                tolerance or tolerance exemption
                                                previously established for the
                                                active ingredient(s); requires:
                                                (1) submission of product-
                                                specific data; or (2) citation
                                                of previously reviewed and
                                                accepted data; or (3) submission
                                                or citation of data generated at
                                                government expense; or (4)
                                                submission or citation of a
                                                scientifically sound rationale
                                                based on publicly available
                                                literature or other relevant
                                                information that addresses the
                                                data requirement; or (5)
                                                submission of a request for a
                                                data requirement to be waived
                                                supported by a scientifically
                                                sound rationale explaining why
                                                the data requirement does not
                                                apply.
B673.........................             123  New product MUP/EP; unregistered               10           4,863
                                                source of active ingredient(s);
                                                citation of Technical Grade
                                                Active Ingredient (TGAI) data
                                                previously reviewed and accepted
                                                by the Agency. Requires an
                                                Agency determination that the
                                                cited data supports the new
                                                product.
B674.........................             124  New product MUP; Repack of                      4           1,217
                                                identical registered end-use
                                                product as a manufacturing-use
                                                product; same registered uses
                                                only.
B675.........................             125  New product MUP; registered                    10           8,683
                                                source of active ingredient;
                                                submission of completely new
                                                generic data package; registered
                                                uses only.
B676.........................             126  New product; more than one active              13           8,683
                                                ingredient where one active
                                                ingredient is an unregistered
                                                source; product chemistry data
                                                must be submitted; requires: (1)
                                                Submission of product-specific
                                                data, and (2) citation of
                                                previously reviewed and accepted
                                                data; or (3) submission or
                                                citation of data generated at
                                                government expense; or (4)
                                                submission or citation of a
                                                scientifically sound rationale
                                                based on publicly available
                                                literature or other relevant
                                                information that addresses the
                                                data requirement; or (5)
                                                submission of a request for a
                                                data requirement to be waived
                                                supported by a scientifically
                                                sound rationale explaining why
                                                the data requirement does not
                                                apply.
B677.........................             127  New end-use non-food animal                    10           8,400
                                                product with submission of two
                                                or more target animal safety
                                                studies; includes data and/or
                                                waivers of data for only:
                                                product chemistry and/or
                                                acute toxicity and/or...
                                                public health pest
                                                efficacy and/or.
                                                animal safety studies
                                                and/or.
                                                child resistant
                                                packaging.
----------------------------------------------------------------------------------------------------------------


   Table 14--Biopesticides and Pollution Prevention Division--Microbial and Biochemical Pesticides; Amendments
----------------------------------------------------------------------------------------------------------------
                                                                                                     FY '14/15
                                                                                     Decision      registration
           EPA No.               New CR No.                  Action                 review time     service fee
                                                                                     (months)           ($)
----------------------------------------------------------------------------------------------------------------
B621.........................             128  Amendment; Experimental Use                     7           4,863
                                                Permit; no change to an
                                                established temporary tolerance
                                                or tolerance exemption.
B622.........................             129  Amendment; Experimental Use                    11          12,156
                                                Permit; petition to amend an
                                                established or temporary
                                                tolerance or tolerance exemption.
B641.........................             130  Amendment of an established                    13          12,156
                                                tolerance or tolerance exemption.
B680.........................             131  Amendment; registered source of                 5           4,863
                                                active ingredient(s); no new
                                                use(s); no changes to an
                                                established tolerance or
                                                tolerance exemption. Requires
                                                data submission.
B681.........................             132  Amendment; unregistered source of               7           5,789
                                                active ingredient(s). Requires
                                                data submission.
B683.........................             133  Label amendment; requires review/               6           4,863
                                                update of previous risk
                                                assessment(s) without data
                                                submission (e.g., labeling
                                                changes to REI, PPE, PHI).
B684.........................             134  Amending non-food animal product                8           8,400
                                                that includes submission of
                                                target animal safety data;
                                                previously registered.
----------------------------------------------------------------------------------------------------------------


[[Page 59356]]


    Table 15--Biopesticides and Pollution Prevention Division--Straight Chain Lepidopteran Pheromones (SCLPS)
----------------------------------------------------------------------------------------------------------------
                                                                                                     FY '14/15
                                                                                     Decision      registration
           EPA No.               New CR No.                  Action                 review time     service fee
                                                                                     (months)           ($)
----------------------------------------------------------------------------------------------------------------
B690.........................             135  New active ingredient; food or                  7           2,432
                                                non-food use.
B700.........................             136  Experimental Use Permit                         7           1,217
                                                application; new active
                                                ingredient or new use.
B701.........................             137  Extend or amend Experimental Use                4           1,217
                                                Permit.
B710.........................             138  New product; registered source of               4           1,217
                                                active ingredient(s); identical
                                                or substantially similar in
                                                composition and use to a
                                                registered product; no change in
                                                an established tolerance or
                                                tolerance exemption. No data
                                                review, or only product
                                                chemistry data; cite-all data
                                                citation, or selective data
                                                citation where applicant owns
                                                all required data or
                                                authorization from data owner is
                                                demonstrated. Category includes
                                                100% re-package of registered
                                                end-use or manufacturing-use
                                                product that requires no data
                                                submission or data matrix.
B720.........................             139  New product; registered source of               5           1,217
                                                active ingredient(s); requires:
                                                (1) submission of product-
                                                specific data; or (2) citation
                                                of previously reviewed and
                                                accepted data; or (3) submission
                                                or citation of data generated at
                                                government expense; or (4)
                                                submission or citation of a
                                                scientifically sound rationale
                                                based on publicly available
                                                literature or other relevant
                                                information that addresses the
                                                data requirement; or (5)
                                                submission of a request for a
                                                data requirement to be waived
                                                supported by a scientifically
                                                sound rationale explaining why
                                                the data requirement does not
                                                apply.
B721.........................             140  New product; unregistered source                7           2,548
                                                of active ingredient.
B722.........................             141  New use and/or amendment;                       7           2,359
                                                petition to establish a
                                                tolerance or tolerance exemption.
B730.........................             142  Label amendment requiring data                  5           1,217
                                                submission.
----------------------------------------------------------------------------------------------------------------


                    Table 16--Biopesticides and Pollution Prevention Division--Other Actions
----------------------------------------------------------------------------------------------------------------
                                                                                                     FY '14/15
                                                                                     Decision      registration
           EPA No.               New CR No.                  Action                 review time     service fee
                                                                                     (months)           ($)
----------------------------------------------------------------------------------------------------------------
B614.........................             143  Conditional ruling on pre-                      3           2,409
                                                application study waivers;
                                                applicant-initiated.
B615.........................             144  Rebuttal of agency reviewed                     3           2,409
                                                protocol, applicant-initiated.
B682.........................             145  Protocol review; applicant-                     3           2,316
                                                initiated; excludes time for
                                                HSRB review.
----------------------------------------------------------------------------------------------------------------


        Table 17--Biopesticides and Pollution Prevention Division--Plant Incorporated Protectants (PIPS)
----------------------------------------------------------------------------------------------------------------
                                                                                                     FY '14/15
                                                                                     Decision      registration
           EPA No.               New CR No.                  Action                 review time     service fee
                                                                                     (months)           ($)
----------------------------------------------------------------------------------------------------------------
B740.........................             146  Experimental Use Permit                         6          91,165
                                                application; no petition for
                                                tolerance/tolerance exemption.
                                                Includes:
                                               1. non-food/feed use(s) for a new
                                                or registered PIP;.
                                               2. food/feed use(s) for a new or
                                                registered PIP with crop
                                                destruct;.
                                               3. food/feed use(s) for a new or
                                                registered PIP in which an
                                                established tolerance/tolerance
                                                exemption exists for the
                                                intended use(s).
B750.........................             147  Experimental Use Permit                         9         121,552
                                                application; with a petition to
                                                establish a temporary or
                                                permanent tolerance/tolerance
                                                exemption for the active
                                                ingredient. Includes new food/
                                                feed use for a registered PIP.
B770.........................             148  Experimental Use Permit                        15         182,327
                                                application; new PIP; with
                                                petition to establish a
                                                temporary tolerance/tolerance
                                                exemption for the active
                                                ingredient; credit 75% of B771
                                                fee toward registration
                                                application for a new active
                                                ingredient that follows; SAP
                                                review.
B771.........................             149  Experimental Use Permit                        10         121,552
                                                application; new PIP; with
                                                petition to establish a
                                                temporary tolerance/tolerance
                                                exemption for the active
                                                ingredient; credit 75% of B771
                                                fee toward registration
                                                application for a new active
                                                ingredient that follows.
B772.........................             150  Application to amend or extend an               3          12,156
                                                Experimental Use Permit; no
                                                petition since the established
                                                tolerance/tolerance exemption
                                                for the active ingredient is
                                                unaffected.
B773.........................             151  Application to amend or extend an               5          30,390
                                                Experimental Use Permit; with
                                                petition to extend a temporary
                                                tolerance/tolerance exemption
                                                for the active ingredient.
B780.........................             152  Registration application; new                  12         151,940
                                                PIP; non-food/feed.

[[Page 59357]]

 
B790.........................             153  Registration application; new                  18         212,715
                                                PIP; non-food/feed; SAP review.
B800.........................             154  Registration application; new                  12         243,165
                                                PIP; with petition to establish
                                                permanent tolerance/tolerance
                                                exemption for the active
                                                ingredient based on an existing
                                                temporary tolerance/tolerance
                                                exemption.
B810.........................             155  Registration application; new                  18         303,878
                                                PIP; with petition to establish
                                                permanent tolerance/tolerance
                                                exemption for the active
                                                ingredient based on an existing
                                                temporary tolerance/tolerance
                                                exemption. SAP review.
B820.........................             156  Registration application; new                  15         303,878
                                                PIP; with petition to establish
                                                or amend a permanent tolerance/
                                                tolerance exemption of an active
                                                ingredient.
B840.........................             157  Registration application; new                  21         364,653
                                                PIP; with petition to establish
                                                or amend a permanent tolerance/
                                                tolerance exemption of an active
                                                ingredient. SAP review.
B851.........................             158  Registration application; new                   9         121,552
                                                event of a previously registered
                                                PIP active ingredient(s); no
                                                petition since permanent
                                                tolerance/tolerance exemption is
                                                already established for the
                                                active ingredient(s).
B870.........................             159  Registration application;                       9          36,466
                                                registered PIP; new product; new
                                                use; no petition since a
                                                permanent tolerance/tolerance
                                                exemption is already established
                                                for the active ingredient(s).
B880.........................             160  Registration application;                       9          30,390
                                                registered PIP; new product or
                                                new terms of registration;
                                                additional data submitted; no
                                                petition since a permanent
                                                tolerance/tolerance exemption is
                                                already established for the
                                                active ingredient(s).
B881.........................             161  Registration application;                      15          91,165
                                                registered PIP; new product or
                                                new terms of registration;
                                                additional data submitted; no
                                                petition since a permanent
                                                tolerance/tolerance exemption is
                                                already established for the
                                                active ingredient(s). SAP review.
B883.........................             162  Registration application; new                   9         121,552
                                                PIP, seed increase with
                                                negotiated acreage cap and time-
                                                limited registration; with
                                                petition to establish a
                                                permanent tolerance/tolerance
                                                exemption for the active
                                                ingredient based on an existing
                                                temporary tolerance/tolerance
                                                exemption.
B884.........................             163  Registration application; new                  12         151,940
                                                PIP, seed increase with
                                                negotiated acreage cap and time-
                                                limited registration; with
                                                petition to establish a
                                                permanent tolerance/tolerance
                                                exemption for the active
                                                ingredient.
B885.........................             164  Registration application;                       9          91,165
                                                registered PIP, seed increase;
                                                breeding stack of previously
                                                approved PIPs, same crop; no
                                                petition since a permanent
                                                tolerance/tolerance exemption is
                                                already established for the
                                                active ingredient(s).
B890.........................             165  Application to amend a seed                     9          60,777
                                                increase registration; converts
                                                registration to commercial
                                                registration; no petition since
                                                permanent tolerance/tolerance
                                                exemption is already established
                                                for the active ingredient(s).
B891.........................             166  Application to amend a seed                    15         121,552
                                                increase registration; converts
                                                registration to a commercial
                                                registration; no petition since
                                                a permanent tolerance/tolerance
                                                exemption already established
                                                for the active ingredient(s),
                                                SAP review.
B900.........................             167  Application to amend a                          6          12,156
                                                registration, including actions
                                                such as extending an expiration
                                                date, modifying an IRM plan, or
                                                adding an insect to be
                                                controlled.
B901.........................             168  Application to amend a                         12          72,931
                                                registration, including actions
                                                such as extending an expiration
                                                date, modifying an IRM plan, or
                                                adding an insect to be
                                                controlled. SAP review.
B902.........................             169  PIP Protocol review..............               3           6,079
B903.........................             170  Inert ingredient tolerance                      6          60,777
                                                exemption; e.g., a marker such
                                                as NPT II; reviewed in BPPD.
B904.........................             171  Import tolerance or tolerance                   9         121,552
                                                exemption; processed commodities/
                                                food only (inert or active
                                                ingredient).
----------------------------------------------------------------------------------------------------------------


                     Table 18--Inert Ingredients, External Review and Miscellaneous Actions
----------------------------------------------------------------------------------------------------------------
                                                                                                     FY'14/15
                                                                                     Decision      registration
           EPA No.               New CR No.                  Action                 review time     service fee
                                                                                     (months)           ($)
----------------------------------------------------------------------------------------------------------------
I001.........................             172  Approval of new food use inert                 12          18,900
                                                ingredient.
I002.........................             173  Amend currently approved inert                 10           5,250
                                                ingredient tolerance or
                                                exemption from tolerance; new
                                                data.
I003.........................             174  Amend currently approved inert                  8           3,150
                                                ingredient tolerance or
                                                exemption from tolerance; no new
                                                data.
I004.........................             175  Approval of new non-food use                    8          10,500
                                                inert ingredient.

[[Page 59358]]

 
I005.........................             176  Amend currently approved non-food               8           5,250
                                                use inert ingredient with new
                                                use pattern; new data.
I006.........................             177  Amend currently approved non-food               6           3,150
                                                use inert ingredient with new
                                                use pattern; no new data.
I007.........................             178  Approval of substantially similar               4           1,575
                                                non-food use inert ingredients
                                                when original inert is
                                                compositionally similar with
                                                similar use pattern.
I008.........................             179  Approval of new polymer inert                   5           3,570
                                                ingredient, food use.
I009.........................             180  Approval of new polymer inert                   4           2,940
                                                ingredient, non-food use.
I010.........................             181  Petition to amend a tolerance                   6           1,575
                                                exemption descriptor to add one
                                                or more CASRNs; no new data.
M001.........................             182  Study protocol requiring Human                  9           7,560
                                                Studies Review Board review as
                                                defined in 40 CFR part 26 in
                                                support of an active ingredient.
M002.........................             183  Completed study requiring Human                 9           7,560
                                                Studies Review Board review as
                                                defined in 40 CFR part 26 in
                                                support of an active ingredient.
M003.........................             184  External technical peer review of              12          60,900
                                                new active ingredient, product,
                                                or amendment (e.g., consultation
                                                with FIFRA Scientific Advisory
                                                Panel) for an action with a
                                                decision timeframe of less than
                                                12 months. Applicant-initiated
                                                request based on a requirement
                                                of the Administrator, as defined
                                                by FIFRA section 25(d), in
                                                support of a novel active
                                                ingredient, or unique use
                                                pattern or application
                                                technology. Excludes PIP active
                                                ingredients.
M004.........................             185  External technical peer review of              18          60,900
                                                new active ingredient, product,
                                                or amendment (e.g., consultation
                                                with FIFRA Scientific Advisory
                                                Panel) for an action with a
                                                decision timeframe of greater
                                                than 12 months. Applicant-
                                                initiated request based on a
                                                requirement of the
                                                Administrator, as defined by
                                                FIFRA section 25(d), in support
                                                of a novel active ingredient, or
                                                unique use pattern or
                                                application technology. Excludes
                                                PIP active ingredients.
M005.........................             186  New product: combination,                       9          21,000
                                                contains a combination of active
                                                ingredients from a registered
                                                and/or unregistered source;
                                                conventional, antimicrobial and/
                                                or biopesticide. Requires
                                                coordination with other
                                                regulatory divisions to conduct
                                                review of data, label and/or
                                                verify the validity of existing
                                                data as cited. Only existing
                                                uses for each active ingredient
                                                in the combination product.
M006.........................             187  Request for up to 5 letters of                  1             263
                                                certification (Gold Seal) for
                                                one actively registered product.
M007.........................             188  Request to extend Exclusive Use                12           5,250
                                                of data as provided by FIFRA
                                                section 3(c)(1)(F)(ii).
M008.........................             189  Request to grant Exclusive Use of              10           1,575
                                                data as provided by FIFRA
                                                section 3(c)(1)(F)(vi) for a
                                                minor use, when a FIFRA section
                                                2(ll)(2) determination is
                                                required.
----------------------------------------------------------------------------------------------------------------

V. How to Pay Fees

    Applicants must submit fee payments at the time of application, and 
EPA will reject any application that does not contain evidence that the 
fee has been paid. EPA has developed a Web site at http://www.epa.gov/pesticides/fees/tool/index.htm to help applicants identify the fee 
category and the fee. All fees should be rounded up to the whole 
dollar. Payments may be made by check, bank draft, or money order or 
online with a credit card or wire transfer.

A. Online

    You may pay electronically through the government payment Web site 
www.pay.gov.
    1. From the pay.gov home page, under ``Find Public Forms.''
    2. Select ``search by Agency name.''
    3. On the A-Z Index of Forms page, select ``E.''
    4. Select ``Environmental Protection Agency.''
    5. From the list of forms, select ``Pre-payment of Pesticide 
Registration Improvement Act Fee.''
    6. Complete the form entering the PRIA fee category and fee.
    7. Keep a copy of the pay.gov acknowledgement of payment. A copy of 
the acknowledgement must be printed and attached to the front of the 
application to assure that EPA can match the application with the 
payment.

B. By Check or Money Order

    All payments must be in United States currency by check, bank 
draft, or money order drawn to the order of the Environmental 
Protection Agency. On the check, the applicant must supply in the 
information line either the registration number of the product or the 
company number. A copy of the check must accompany the application to 
the Agency, specifically attached to the front of the application. The 
copy of the check ensures that payment has been made at the time of 
application and will enable the Agency to properly connect the payment 
with the application sent to the Agency.
    If you send the Agency a check, it will be converted into an 
electronic funds transfer (EFT). This means the Agency will copy your 
check and use the account information on it to electronically debit 
your account for the amount of the check. The debit from your account 
will usually occur within 24 hours and will be shown on your regular 
account statement.
    You will not receive your original check back. The Agency will 
destroy your original check but will keep the copy of it. If the EFT 
cannot be processed for technical reasons, you authorize the Agency to 
process the copy in place of your original check. If

[[Page 59359]]

the EFT cannot be completed because of insufficient funds, the Agency 
may try to make the transfer up to two times.
    All paper-based payments should be sent to the following address:
     By U.S. Postal Service. U.S. Environmental Protection 
Agency, Washington Finance Center, FIFRA Service Fees, P.O. Box 979074, 
St. Louis, MO 63197-9000.
     By courier or personal delivery. U.S. Bank, Government 
Lockbox 979074, 1005 Convention Plaza, SL-MO-C2-GL, St. Louis, MO 
63197, (314) 418-4990.

VI. How to Submit Applications

    Submissions to the Agency should be made at the address given in 
Unit VII. The applicant should attach documentation that the fee has 
been paid which may be pay.gov payment acknowledgement or a copy of the 
check. If the applicant is applying for a fee waiver, the applicant 
should provide sufficient documentation as described in FIFRA section 
33(b)(7) and http://www.epa.gov/pesticides/fees/questions/waivers.htm. 
The fee waiver request should be easy to identify and separate from the 
rest of the application and submitted with documentation that at least 
25% of the fee has been paid.
    If evidence of fee payment (electronic acknowledgement or copy of 
check properly identified as to company) is not submitted with the 
application, EPA will reject the application and will not process it 
further.
    After EPA receives an application and payment, EPA performs a 
screen on the application to determine that the category is correct and 
that the proper fee amount has been paid. If either is incorrect, EPA 
will notify the applicant and require payment of any additional amount 
due. A refund will be provided in case of an overpayment. EPA will not 
process the application further until the proper fee has been paid for 
the category of application or a request for a fee waiver accompanies 
the application and the appropriate portion of the fee has been paid.
    EPA will assign a unique identification number to each covered 
application for which payment has been made. EPA notifies the applicant 
of the unique identification number. This information is sent by email 
if EPA has either an email address on file or an email address is 
provided on the application.

VII. Addresses for Applications

    New covered applications should be identified in the title line 
with the mail code REGFEE.
     By U.S. Postal Service mail. Document Processing Desk 
(REGFEE), Office of Pesticide Programs (7504P), U.S. Environmental 
Protection Agency, 1200 Pennsylvania Avenue NW., Washington, DC 20460-
0001.
     By courier. Document Processing Desk (REGFEE), Office of 
Pesticide Programs, U.S. Environmental Protection Agency, Room S-4400, 
One Potomac Yard (South Bldg.), 2777 S. Crystal Drive, Arlington, VA 
22202-4501.
    Couriers and delivery personnel must present a valid picture 
identification card to gain access to the building. Hours of operation 
for the Document Processing Desk are 8 a.m. to 4:30 p.m., Monday 
through Friday, excluding Federal holidays.

List of Subjects

    Environmental protection, Administrative practice and procedure, 
Pesticides.

    Dated: September 18, 2013.
Martha Monell,
Acting Director, Office of Pesticide Programs.
[FR Doc. 2013-23368 Filed 9-25-13; 8:45 am]
BILLING CODE 6560-50-P


