Title 21
PART 343
Part 343 - Internal Analgesic, Antipyretic, And Antirheumatic Drug Products For Over-the-counter Human Use
- Authority: 21 U.S.C. 321, 351, 352, 353, 355, 360, 371.
- Source: 63 FR 56814, Oct. 23, 1998, unless otherwise noted.
| 21:5.0.1.1.20.1 | SUBPART A | Subpart A - General Provisions | |
| 21:5.0.1.1.20.1.1.1 | SECTION 343.1 | 343.1 Scope. | |
| 21:5.0.1.1.20.1.1.2 | SECTION 343.3 | 343.3 Definitions. | |
| 21:5.0.1.1.20.2 | SUBPART B | Subpart B - Active Ingredients | |
| 21:5.0.1.1.20.2.1.1 | SECTION 343.10 | 343.10 [Reserved] | |
| 21:5.0.1.1.20.2.1.2 | SECTION 343.12 | 343.12 Cardiovascular active ingredients. | |
| 21:5.0.1.1.20.2.1.3 | SECTION 343.13 | 343.13 Rheumatologic active ingredients. | |
| 21:5.0.1.1.20.2.1.4 | SECTION 343.20 | 343.20 [Reserved] | |
| 21:5.0.1.1.20.2.1.5 | SECTION 343.22 | 343.22 Permitted combinations of active ingredients for cardiovascular-rheumatologic use. | |
| 21:5.0.1.1.20.3 | SUBPART C | Subpart C - Labeling | |
| 21:5.0.1.1.20.3.1.1 | SECTION 343.50-343.60 | 343.50-343.60 [Reserved] | |
| 21:5.0.1.1.20.3.1.2 | SECTION 343.80 | 343.80 Professional labeling. | |
| 21:5.0.1.1.20.4 | SUBPART D | Subpart D - Testing Procedures | |
| 21:5.0.1.1.20.4.1.1 | SECTION 343.90 | 343.90 Dissolution and drug release testing. |