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U.S. Code Regulations Constitution Journal Apps
  1. Regulations
    All Titles
  2. title 21
    Food and Drugs
  3. chapter I-i3
    CHAPTER I—FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED)
  4. part 201
    PART 201—LABELING
  5. subpart C
    Subpart C—Labeling Requirements for Over-the-Counter Drugs

Subpart C. Subpart C—Labeling Requirements for Over-the-Counter Drugs

  • § 201.60 - Principal display panel.
  • § 201.61 - Statement of identity.
  • § 201.62 - Declaration of net quantity of contents.
  • § 201.63 - Pregnancy/breast-feeding warning.
  • § 201.64 - Sodium labeling.
  • § 201.66 - Format and content requirements for over-the-counter (OTC) drug product labeling.
  • § 201.67 - Labeling requirements for a nonprescription drug product with an additional condition for nonprescription use (ACNU).
  • § 201.70 - Calcium labeling.
  • § 201.71 - Magnesium labeling.
  • § 201.72 - Potassium labeling.
  • § 201.80 - Specific requirements on content and format of labeling for human prescription drug and biological products; older drugs not described in § 201.56(b)(1).
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