Code of Federal Regulations > Title 21 > Chapter I > Part 201 - PART 201—LABELING

U.S. Code of Federal Regulations

Regulations most recently checked for updates: May 24, 2025

Subpart A [§ 201.1 - § 201.26] - Subpart A—General Labeling Provisions

Subpart B [§ 201.50 - § 201.58] - Subpart B—Labeling Requirements for Prescription Drugs and/or Insulin

Subpart C [§ 201.60 - § 201.80] - Subpart C—Labeling Requirements for Over-the-Counter Drugs

Subpart D [§ 201.100 - § 201.130] - Subpart D—Exemptions From Adequate Directions for Use

Subpart E [§ 201.150 - § 201.161] - Subpart E—Other Exemptions

Subpart F [§ 201.200 - § 201.200] - Subpart F—Labeling Claims for Drugs in Drug Efficacy Study

Subpart G [§ 201.300 - § 201.328] - Subpart G—Specific Labeling Requirements for Specific Drug Products