Title 21
PART 350
Part 350 - Antiperspirant Drug Products For Over-the-counter Human Use
- Authority: 21 U.S.C. 321, 351, 352, 353, 355, 360, 371.
- Source: 68 FR 34291, June 9, 2003, unless otherwise noted.
| 21:5.0.1.1.26.1 | SUBPART A | Subpart A - General Provisions | |
| 21:5.0.1.1.26.1.1.1 | SECTION 350.1 | 350.1 Scope. | |
| 21:5.0.1.1.26.1.1.2 | SECTION 350.3 | 350.3 Definition. | |
| 21:5.0.1.1.26.2 | SUBPART B | Subpart B - Active Ingredients | |
| 21:5.0.1.1.26.2.1.1 | SECTION 350.10 | 350.10 Antiperspirant active ingredients. | |
| 21:5.0.1.1.26.3 | SUBPART C | Subpart C - Labeling | |
| 21:5.0.1.1.26.3.1.1 | SECTION 350.50 | 350.50 Labeling of antiperspirant drug products. | |
| 21:5.0.1.1.26.4 | SUBPART D | Subpart D - Guidelines for Effectiveness Testing | |
| 21:5.0.1.1.26.4.1.1 | SECTION 350.60 | 350.60 Guidelines for effectiveness testing of antiperspirant drug products. |