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Regulations last checked for updates: Nov 21, 2024
Title 21 - Food and Drugs last revised: Nov 19, 2024
All Titles
Title 21
Chapter I
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
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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