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 - § 201.130] - 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