
[Federal Register: October 12, 2010 (Volume 75, Number 196)]
[Notices]               
[Page 62545-62546]
From the Federal Register Online via GPO Access [wais.access.gpo.gov]
[DOCID:fr12oc10-85]                         

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DEPARTMENT OF HEALTH AND HUMAN SERVICES

Food and Drug Administration

[Docket No. FDA-2010-F-0510]

 
Ferm Solutions, Inc.; Filing of Food Additive Petition (Animal 
Use); Virginiamycin

AGENCY: Food and Drug Administration, HHS.

ACTION: Notice.

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SUMMARY: The Food and Drug Administration (FDA) is announcing that Ferm 
Solutions, Inc. has filed a petition proposing that the food additive 
regulations be amended to provide for the safe use of virginiamycin as 
an antimicrobial processing aid in fuel-ethanol fermentations with 
respect to its consequent presence in by-product distiller grains used 
as an animal feed or feed ingredient.

DATES: Submit either electronic or written comments on the petitioner's 
environmental assessment by November 12, 2010.

ADDRESSES: Submit electronic comments to: http://www.regulations.gov. 
Submit written comments to the Division of Dockets Management (HFA-
305), Food and Drug Administration, 5630 Fishers Lane, Rm. 1061, 
Rockville, MD 20852.

FOR FURTHER INFORMATION CONTACT: Isabel W. Pocurull, Center for 
Veterinary Medicine, Food and Drug Administration, 7519 Standish Pl., 
Rockville, MD 20855, 240-453-6853, e-mail: isabel.pocurull@fda.hhs.gov.

SUPPLEMENTARY INFORMATION: Under the Federal Food, Drug, and Cosmetic 
Act (section 409(b)(5) (21 U.S.C. 348(b)(5)), notice is given that a 
food additive petition (FAP 2264) has been filed by Ferm Solutions, 
Inc., PO Box 203, Danville, KY 40422. The petition proposes to amend 
the food additive regulations in part 573 Food Additives Permitted in 
Feed and Drinking Water of Animals (21 CFR part 573) to provide for the 
safe use of virginiamycin as an antimicrobial processing aid in fuel-
ethanol fermentations with respect to its consequent presence in by-
product distiller grains used as an animal feed or feed ingredient.
    The potential environmental impact of this action is being 
reviewed. To encourage public participation consistent with regulations 
issued under the National Environmental Policy Act (40 CFR 1501.4(b)), 
the agency is placing the environmental assessment submitted with the 
petition that is the subject of this notice on public display at the 
Division of Dockets Management (see DATES and ADDRESSES) for public 
review and comment.
    Interested persons may submit to the Division of Dockets Management 
(see ADDRESSES) either electronic or written comments regarding this 
document. It is only necessary to send one set of comments. It is no 
longer necessary to send two copies of mailed comments. Identify 
comments with the docket number found in brackets in the heading of 
this document. Received comments may be seen in the Division of Dockets 
Management between 9 a.m. and 4 p.m., Monday through Friday. FDA will 
also place on public display any amendments to, or comments on, the 
petitioner's environmental assessment without further announcement in 
the Federal Register. If, based on its review, the agency finds that an 
environmental impact statement is not required and this petition 
results in a regulation, the notice of availability of the agency's 
finding of no significant impact and the evidence supporting that 
finding will be published with the regulation in the Federal Register 
in accordance with 21 CFR 25.51(b).


[[Page 62546]]


    Dated: October 4, 2010.
Bernadette Dunham,
Director, Center for Veterinary Medicine.
[FR Doc. 2010-25522 Filed 10-8-10; 8:45 am]
BILLING CODE 4160-01-P

