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

Document ID: FDA-1978-N-0018-0700
Document Type: Notice
Agency: Food And Drug Administration
Topics: No Topics associated with this document
Federal Register Number: C1-2011-14766
CFR Citation: 21 CFR Part 201
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Details Information

Document Subtype: Correction
Received Date: July 05 2011, at 12:00 AM Eastern Daylight Time
Start-End Page: 38975 - 38975
Page Count: 1
Comment Start Date: July 5 2011, at 12:00 AM Eastern Standard Time

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