21 C.F.R. § 111.120

What quality control operations are required for components, packaging, and labels before use in the manufacture of a dietary supplement?

Last amended: 2016Year: 2026Length: 102 wordsSubsections: 5Official source

Cite as 21 C.F.R. § 111.120 (2026)

Quality control operations for components, packaging, and labels before use in the manufacture of a dietary supplement must include: (a) Reviewing all receiving records for components, packaging, and labels; (b) Determining whether all components, packaging, and labels conform to specifications established under § 111.70 (b) and (d); (c) Conducting any required material review and making any required disposition decision; (d) Approving or rejecting any treatment and in-process adjustments of components, packaging, or labels to make them suitable for use in the manufacture of a dietary supplement; and (e) Approving, and releasing from quarantine, all components, packaging, and labels before they are used.
Cross-references to the CFR
111.70
21 C.F.R. § 111.120: What quality control operations are required for components, packaging, and labels before use in the manufacture of a dietary supplement? | Justis AI