Labeling and Effectiveness Testing: Sunscreen Drug Products for Over-the-Counter Human Use - Notice of Correction

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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:

Regulatory Text

§ 201.327 [Corrected]

In § 201.327, on page 35661, in the third column, § 201.327(i)(1)(ii)(A)(2) and (3) should read as follows:

(2) V i (λ) = 10 0.094 * ( 298 -λ) (298 < λ ≤ 328 nm)

(3) V i (λ) = 10 0.015 * ( 140 -λ) (328 < λ ≤ 400 nm)

[FR Doc. C1-2011-14766 Filed 7-1-11; 8:45 am]
BILLING CODE 1505-01-D
 
 
Comment Period Closed
ID: FDA-1978-N-0018-0700
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Document Information

Date Posted: Jul 5, 2011
RIN: 0910-AF43
CFR: 21 CFR Part 201
Federal Register Number: C1-2011-14766
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