 |
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 335 - Antidiarrheal Drug Products for over-the-Counter Human Use |
| Subpart A - General Provisions |
| § 335.1 - Scope. |
| § 335.3 - Definitions. |
| Subpart B - Active Ingredients |
| § 335.10 - Antidiarrheal active ingredients. |
| Subpart C - Labeling |
| § 335.50 - Labeling of antidiarrheal drug products. |