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Code · CFR · Title 21 — Food and Drugs · Part 111 — Current Good Manufacturing Practice in Manufacturing, Packaging, Labeling, or Holding Operations for Dietary Supplements · § 111.420

§ 111.420. What requirements apply to repackaging and relabeling?

75 words·~1 min read·/us/cfr/t21/s§ 111.420·

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(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.
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