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U.S. Code of Federal Regulations
Regulations most recently checked for updates: Oct 03, 2023
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Title 21
Chapter I
Part 201 - PART 201—LABELING
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 - § 201.129] - 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
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