Federal (United States) · Regulations
Subpart C
10 sections
10 sections
- 21 C.F.R. § 201.60Principal display panel.
- 21 C.F.R. § 201.61Statement of identity.
- 21 C.F.R. § 201.62Declaration of net quantity of contents.
- 21 C.F.R. § 201.64Sodium labeling.
- 21 C.F.R. § 201.66Format and content requirements for over-the-counter (OTC) drug product labeling.
- 21 C.F.R. § 201.67Labeling requirements for a nonprescription drug product with an additional condition for nonprescription use (ACNU).
- 21 C.F.R. § 201.70Calcium labeling.
- 21 C.F.R. § 201.71Magnesium labeling.
- 21 C.F.R. § 201.72Potassium labeling.
- 21 C.F.R. § 201.80Specific requirements on content and format of labeling for human prescription drug and biological products; older drugs not described in § 201.56(b)(1).