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Anorectal Drug Products for Over-the-Counter Human Use

other · Food and Drug Administration · Rule · Published 2003-08-26 · Effective 2003-09-25 · 68 FR 51167

Document

Document number
03-21749
Federal Register citation
68 FR 51167
CFR reference
21 CFR 310
Type
Rule
Action
Final rule.
Category
other
Sub-agency
Food and Drug Administration
Publication date
2003-08-26
Effective date
2003-09-25
HHS docket
Docket No. 1980N-0050

Abstract

The Food and Drug Administration (FDA) is issuing a final rule establishing that any over-the-counter (OTC) drug product containing a combination of hydrocortisone and pramoxine hydrochloride (HCl) for anorectal use is not generally recognized as safe and effective and is misbranded. This combination product is not currently marketed OTC. This final rule discusses data on the combination of hydrocortisone and pramoxine HCl that were still under review when an earlier final rule on OTC anorectal drug products was issued. This rule is part of FDA's ongoing review of OTC drug products.

Source

Authoritative
Federal Register document
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