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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 349 - Ophthalmic Drug Products for over-the-Counter Human Use |
| Subpart A - General Provisions |
| § 349.1 - Scope. |
| § 349.3 - Definitions. |
| Subpart B - Active Ingredients |
| § 349.10 - Ophthalmic astringent. |
| § 349.12 - Ophthalmic demulcents. |
| § 349.14 - Ophthalmic emollients. |
| § 349.16 - Ophthalmic hypertonicity agent. |
| § 349.18 - Ophthalmic vasoconstrictors. |
| § 349.20 - Eyewashes. |
| § 349.30 - Permitted combinations of active ingredients. |
| Subpart C - Labeling |
| § 349.50 - Labeling of ophthalmic drug products. |
| § 349.55 - Labeling of ophthalmic astringent drug products. |
| § 349.60 - Labeling of ophthalmic demulcent drug products. |
| § 349.65 - Labeling of ophthalmic emollient drug products. |
| § 349.70 - Labeling of ophthalmic hypertonicity drug products. |
| § 349.75 - Labeling of ophthalmic vasoconstrictor drug products. |
| § 349.78 - Labeling of eyewash drug products. |
| § 349.79 - Labeling of permitted combinations of active ingredients. |
| § 349.80 - Professional labeling. |