# Sunscreen Drug Products for Over-the-Counter Human Use; Final Monograph; Technical Amendment
> **Food and Drug Administration** · Final rule; technical amendment. · Published 2002-06-20 · Effective 2002-09-01 · 67 FR 41821
## Document
- **Document number:** 01-15632
- **Category:** other
- **Sub-agency:** Food and Drug Administration
- **Federal Register citation:** 67 FR 41821
- **CFR reference:** 21 CFR 352
- **Publication date:** 2002-06-20
- **Effective date:** 2002-09-01
- **HHS docket:** Docket No. 78N-0038
## Abstract

The Food and Drug Administration (FDA) is amending the regulation that established conditions under which over-the-counter (OTC) sunscreen drug products are generally recognized as safe and effective and not misbranded. This amendment updates the monograph to incorporate United States Pharmacopeia (U.S.P.) name changes for four active ingredients included in the monograph. This final rule is part of FDA's ongoing review of OTC drug products.

## Source
- [Federal Register document](https://www.federalregister.gov/documents/2002/06/20/01-15632/sunscreen-drug-products-for-over-the-counter-human-use-final-monograph-technical-amendment)
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