21 CFR § 111.420 Current Good Manufacturing Practice in Manufacturing, Packaging, Labeling, or Holding Operations for Dietary Supplements

§ 111.420 What requirements apply to repackaging and relabeling?

Current through Sep 8, 2026 · Read all of Part 111

(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.

← § 111.415 What requirements apply to filling, assembling, packaging, labeling, and related operations?§ 111.425 What requirements apply to a packaged and labeled dietary supplement that is rejected for distribution? →