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Regulations last checked for updates: May 22, 2025

Title 21 - Food and Drugs last revised: May 19, 2025
All TitlesTitle 21Chapter IPart 349 - PART 349—OPHTHALMIC DRUG PRODUCTS FOR OVER-THE-COUNTER HUMAN USE
  • Subpart A [§ 349.1 - § 349.3] - Subpart A—General Provisions
  • Subpart B [§ 349.10 - § 349.30] - Subpart B—Active Ingredients
  • Subpart C [§ 349.50 - § 349.80] - Subpart C—Labeling
authority: 21 U.S.C. 321,351,352,353,355,360,371
source: 53 FR 7090, Mar. 4, 1988, unless otherwise noted.
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