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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 801Subpart C - Subpart C—Labeling Requirements for Over-the-Counter Devices
  • § 801.60 - Principal display panel.
  • § 801.61 - Statement of identity.
  • § 801.62 - Declaration of net quantity of contents.
  • § 801.63 - Medical devices; warning statements for devices containing or manufactured with chlorofluorocarbons and other class I ozone-depleting substances.
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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