
[Federal Register: July 5, 2011 (Volume 76, Number 128)]
[Rules and Regulations]               
[Page 38975]
From the Federal Register Online via GPO Access [wais.access.gpo.gov]
[DOCID:fr05jy11-2]                         

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

DEPARTMENT OF HEALTH AND HUMAN SERVICES

Food and Drug Administration

21 CFR Part 201

[Docket No. FDA-1978-N-0018] (formerly Docket No. 1978N-0038)
RIN 0910-AF43

 
Labeling and Effectiveness Testing; Sunscreen Drug Products for 
Over-the-Counter Human Use

Correction

    In rule document 2011-14766 appearing on pages 35620-35665 in the 
issue of Friday, June 17, 2011, make the following correction:


Sec.  201.327  [Corrected]

    In Sec.  201.327, on page 35661, in the third column, Sec.  
201.327(i)(1)(ii)(A)(2) and (3) should read as follows:
    (2) Vi ([lambda]) = 10\0.094\ * (\298\-
[lgr]) (298 < [lgr] <= 328 nm)
    (3) Vi ([lambda]) = 10\0.015\ * (\140\-
[lgr]) (328 < [lgr] <= 400 nm)

[FR Doc. C1-2011-14766 Filed 7-1-11; 8:45 am]
BILLING CODE 1505-01-D

