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Labeling Requirements for Over-the-Counter Drugs | Midpage
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Code of Federal Regulations
Title 21
Chapter I
Subchapter C
Part 201
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).