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Code of Federal Regulations (Last Updated: October 10, 2024) |
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Title 21 - Food and Drugs |
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Chapter I - Food and Drug Administration, Department of Health and Human Services |
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SubChapter C - Drugs: General |
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Part 201 - Labeling |
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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. |
| § 201.70 - 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). |