21 CFR Part 352
PART 352—SUNSCREEN DRUG PRODUCTS FOR OVER-THE-COUNTER HUMAN USE [STAYED INDEFINITELY]
- PART 352—SUNSCREEN DRUG PRODUCTS FOR OVER-THE-COUNTER HUMAN USE [STAYED INDEFINITELY]
- Chapter I—Food and Drug Administration, Department of Health and Human Services › Subchapter D—Drugs for Human Use
- 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.
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