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Regulations last checked for updates: May 14, 2025
Title 21 - Food and Drugs last revised: May 12, 2025
All Titles
Title 21
Chapter I
Part 201
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 - xxx
§ 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).
authority:
21 U.S.C. 321
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42 U.S.C. 216
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241
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source:
40 FR 13998, Mar. 27, 1975, unless otherwise noted.
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