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

  1. Subpart A—General Provisions (§§ 352.1 - 352.3)
  2. Subpart B—Active Ingredients (§§ 352.10 - 352.20)
  3. Subpart C—Labeling (§§ 352.50 - 352.60)
  4. Subpart D—Testing Procedures (§§ 352.70 - 352.77)
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.