 |
Code of Federal Regulations (Last Updated: November 8, 2024) |
 |
Title 21 - Food and Drugs |
|
|
Chapter I - Food and Drug Administration, Department of Health and Human Services |
|
|
SubChapter D - Drugs for Human Use |
|
|
Part 350 - Antiperspirant Drug Products for over-the-Counter Human Use |
| Subpart A - General Provisions |
| § 350.1 - Scope. |
| § 350.3 - Definition. |
| Subpart B - Active Ingredients |
| § 350.10 - Antiperspirant active ingredients. |
| Subpart C - Labeling |
| § 350.50 - Labeling of antiperspirant drug products. |
| Subpart D - Guidelines for Effectiveness Testing |
| § 350.60 - Guidelines for effectiveness testing of antiperspirant drug products. |