e-CFR banner

Home
gpo.gov
govinfo.gov

e-CFR Navigation Aids

Browse

Simple Search

Advanced Search

 — Boolean

 — Proximity

 

Search History

Search Tips

Corrections

Latest Updates

User Info

FAQs

Agency List

Incorporation By Reference

eCFR logo

Related Resources

 

Electronic Code of Federal Regulations

e-CFR data is current as of April 2, 2020

Title 21Chapter ISubchapter DPart 349


TITLE 21—Food and Drugs

CHAPTER I—FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED)

SUBCHAPTER D—DRUGS FOR HUMAN USE

PART 349—OPHTHALMIC DRUG PRODUCTS FOR OVER-THE-COUNTER HUMAN USE

rule

Subpart A—GENERAL PROVISIONS

§349.1
Scope.
§349.3
Definitions.
rule

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.
rule

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.

Need assistance?