PART 352—SUNSCREEN DRUG PRODUCTS FOR OVER-THE-COUNTER HUMAN USE [STAYED INDEFINITELY]
- SUBPART A—General Provisions (§352.1 to §352.3)
- SUBPART B—Active Ingredients (§352.10 to §352.20)
- SUBPART C—Labeling (§352.50 to §352.60)
- SUBPART D—Testing Procedures (§352.70 to §352.77)