part_subject: "CURRENT GOOD MANUFACTURING PRACTICE IN MANUFACTURING, PACKAGING, LABELING, OR HOLDING OPERATIONS FOR DIETARY SUPPLEMENTS"
subpart_code: "L"
subpart_subject: "Production and Process Control System: Requirements for Packaging and Labeling Operations"
section_number: "111.420"
section_subject: "What requirements apply to repackaging and relabeling?"
cfr_reference: "21 CFR 111.420"
title_name: "Title 21"
title_subject: "Food and Drugs"
parts_covered: "Parts 100 to 169"
revised_date: "Revised as of April 1, 2019"
publication_date: "As of April 1, 2019"
contains_description: "Containing a codification of documents of general applicability and future effect"
publication_info: "Published by the Office of the Federal Register National Archives and Records Administration as a Special Edition of the Federal Register"
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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.