21 CFR Part 349
PART 349—OPHTHALMIC DRUG PRODUCTS FOR OVER-THE-COUNTER HUMAN USE
- PART 349—OPHTHALMIC DRUG PRODUCTS FOR OVER-THE-COUNTER HUMAN USE
- Chapter I—Food and Drug Administration, Department of Health and Human Services › Subchapter D—Drugs for 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.
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