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Regulations last checked for updates: May 14, 2025

Title 21 - Food and Drugs last revised: May 12, 2025
All TitlesTitle 21Chapter IPart 801 - PART 801—LABELING
  • Subpart A [§ 801.1 - § 801.18] - Subpart A—General Labeling Provisions
  • Subpart B [§ 801.20 - § 801.57] - Subpart B—Labeling Requirements for Unique Device Identification
  • Subpart C [§ 801.60 - § 801.63] - Subpart C—Labeling Requirements for Over-the-Counter Devices
  • Subpart D [§ 801.109 - § 801.128] - Subpart D—Exemptions From Adequate Directions for Use
  • Subpart E [§ 801.150 - § 801.150] - Subpart E—Other Exemptions
  • Subpart F - Subparts F-G [Reserved]
  • Subpart H [§ 801.405 - § 801.437] - Subpart H—Special Requirements for Specific Devices
authority: 21 U.S.C. 321,331,351,352,360d,360i,360j,371,374
source: 41 FR 6896, Feb. 13, 1976, unless otherwise noted.
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