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21 CFR 111.83

§ 111.83 What are the requirements for reserve samples?

United States · 21 CFR — Food and Drugs · Status: effective

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21 CFR 111.83, § 111.83 What are the requirements for reserve samples?, United States, version 1 as recorded 2026-07-09, yourstate.us, https://yourstate.us/provision/84152
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Full text

(a) You must collect and hold reserve samples of each lot of packaged and labeled dietary supplements that you distribute. (b) The reserve samples must: (1) Be held using the same container-closure system in which the packaged and labeled dietary supplement is distributed, or if distributing dietary supplements to be packaged and labeled, using a container-closure system that provides essentially the same characteristics to protect against contamination or deterioration as the one in which it is distributed for packaging and labeling elsewhere; (2) Be identified with the batch, lot, or control number; (3) Be retained for 1 year past the shelf life date (if shelf life dating is used), or for 2 years from the date of distribution of the last batch of dietary supplements associated with the reserve sample, for use in appropriate investigations; and (4) Consist of at least twice the quantity necessary for all tests or examinations to determine whether or not the dietary supplement meets product specifications.

Legislative history

This is a federal regulation, adopted through agency rulemaking under the Administrative Procedure Act — not enacted by a recorded vote of Congress.