21 CFR 111.420
§ 111.420 What requirements apply to repackaging and relabeling?
United States · 21 CFR — Food and Drugs · Status: effective
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- Citation
- 21 CFR 111.420, § 111.420 What requirements apply to repackaging and relabeling?, United States, version 1 as recorded 2026-07-09, yourstate.us, https://yourstate.us/provision/84198
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Full text
(a) You may repackage or relabel dietary supplements only after quality control personnel have approved such repackaging or relabeling.
(b) You must examine a representative sample of each batch of repackaged or relabeled dietary supplements to determine whether the repackaged or relabeled dietary supplements meet all specifications established in accordance with § 111.70(g).
(c) Quality control personnel must approve or reject each batch of repackaged or relabeled dietary supplement prior to its release for distribution.
Legislative history
This is a federal regulation, adopted through agency rulemaking under the Administrative Procedure Act — not enacted by a recorded vote of Congress.