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

other · Food and Drug Administration · Rule · Published 2011-07-05 · 76 FR 38975

Document

Document number
C1-2011-14766
Federal Register citation
76 FR 38975
CFR reference
21 CFR 201
Type
Rule
Action
Category
other
Sub-agency
Food and Drug Administration
Publication date
2011-07-05
HHS docket
Docket No. FDA-1978-N-0018

Source

Authoritative
Federal Register document
Machine
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