CFR - Code of Federal Regulations Title 21

The information on this page is current as of Dec 22, 2023.

For the most up-to-date version of CFR Title 21, go to the Electronic Code of Federal Regulations (eCFR).

TITLE 21--FOOD AND DRUGS
CHAPTER I--FOOD AND DRUG ADMINISTRATION
DEPARTMENT OF HEALTH AND HUMAN SERVICES
SUBCHAPTER D - DRUGS FOR HUMAN USE

PART 352 SUNSCREEN DRUG PRODUCTS FOR OVER-THE-COUNTER HUMAN USE [STAYED INDEFINITELY]

Subpart A - General Provisions
   § 352.1 - Scope.
   § 352.3 - Definitions.

Subpart B - Active Ingredients
   § 352.10 - Sunscreen active ingredients.
   § 352.20 - Permitted combinations of active ingredients.

Subpart C - Labeling
   § 352.50 - Principal display panel of all sunscreen drug products.
   § 352.52 - Labeling of sunscreen drug products.
   § 352.60 - Labeling of permitted combinations of active ingredients.

Subpart D - Testing Procedures
   § 352.70 - Standard sunscreen.
   § 352.71 - Light source (solar simulator).
   § 352.72 - General testing procedures.
   § 352.73 - Determination of SPF value.
   § 352.76 - Determination if a product is water resistant or very water resistant.
   § 352.77 - Test modifications.

Authority: 21 U.S.C. 321, 351, 352, 353, 355, 360, 371.
Source: 64 FR 27687, May 21, 1999, unless otherwise noted.