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Code of Federal Regulations (Last Updated: November 8, 2024) |
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Title 21 - Food and Drugs |
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Chapter I - Food and Drug Administration, Department of Health and Human Services |
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SubChapter D - Drugs for Human Use |
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Part 332 - Antiflatulent Products for over-the-Counter Human Use |
| Subpart A - General Provisions |
| § 332.1 - Scope. |
| § 332.3 - Definitions. |
| Subpart B - Active Ingredients |
| § 332.10 - Antiflatulent active ingredients. |
| § 332.15 - Combination with non-antiflatulent active ingredients. |
| Subpart C - Labeling |
| § 332.30 - Labeling of antiflatulent drug products. |
| § 332.31 - Professional labeling. |
| Subpart D - Labeling |