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U.S. Department of Health and Human Services

CFR - Code of Federal Regulations Title 21

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The information on this page is current as of Dec 22, 2023.

For the most up-to-date version of CFR Title 21, go to the Electronic Code of Federal Regulations (eCFR).

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TITLE 21--FOOD AND DRUGS
CHAPTER I--FOOD AND DRUG ADMINISTRATION
DEPARTMENT OF HEALTH AND HUMAN SERVICES
SUBCHAPTER D - DRUGS FOR HUMAN USE
 
PART 349OPHTHALMIC 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.

Authority: 21 U.S.C. 321, 351, 352, 353, 355, 360, 371.
Source: 53 FR 7090, Mar. 4, 1988, unless otherwise noted.

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