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Code of Federal Regulations (Last Updated: November 8, 2024) |
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Title 21 - Food and Drugs |
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Chapter I - Food and Drug Administration, Department of Health and Human Services |
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SubChapter D - Drugs for Human Use |
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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. |