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  1. Regulations
    All Titles
  2. title 21
    Food and Drugs
  3. chapter I-i7
    CHAPTER I—FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED)
  4. part 801
    PART 801—LABELING

Part 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
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