21 CFR 111.120
§ 111.120 What quality control operations are required for components, packaging, and labels before use in the manufacture of a dietary supplement?
United States · 21 CFR — Food and Drugs · Status: effective
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- Citation
- 21 CFR 111.120, § 111.120 What quality control operations are required for components, packaging, and labels before use in the manufacture of a dietary supplement?, United States, version 1 as recorded 2026-07-09, yourstate.us, https://yourstate.us/provision/84162
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Full text
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.
Legislative history
This is a federal regulation, adopted through agency rulemaking under the Administrative Procedure Act — not enacted by a recorded vote of Congress.