StacksVerified U.S. regulatory reference

21 CFR §111.120

Verified against eCFR.gov as of June 20, 2026View official text on eCFR.gov ↗
Quality control operations for components, packaging, and labels before use in the manufacture of a dietary supplement must include:
  1. (a)Reviewing all receiving records for components, packaging, and labels;
  2. (b)Determining whether all components, packaging, and labels conform to specifications established under § 111.70 (b) and (d);
  3. (c)Conducting any required material review and making any required disposition decision;
  4. (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
  5. (e)Approving, and releasing from quarantine, all components, packaging, and labels before they are used.