Part 352 — Sunscreen Drug Products for Over-the-Counter Human Use [Stayed Indefinitely]
Current through Sep 8, 2026
Authority: 21 U.S.C. 321, 351, 352, 353, 355, 360, 371.
Source: 64 FR 27687, May 21, 1999, unless otherwise noted.
Effective Date Note:
At 68 FR 33381, June 4, 2003, part 352 was stayed until further notice, effective June 4, 2004.
Sections
- § 352.1 Scope.
- § 352.3 Definitions.
- § 352.10 Sunscreen active ingredients.
- § 352.20 Permitted combinations of active ingredients.
- § 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.
- § 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.