Code of Federal Regulations · Section
§ 111.170 — What Requirements Apply To Rejected Components, Packaging, And Labels, And To Rejected Products That Are Received For Packaging Or Labeling As A Dietary Supplement?
21 C.F.R. § 111.170
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You must clearly identify, hold, and control under a quarantine system for appropriate disposition any component, packaging, and label, and any product that you receive for packaging or labeling as a dietary supplement (and for distribution rather than for return to the supplier), that is rejected and unsuitable for use in manufacturing, packaging, or labeling operations.
Authorizing Statute
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Regulations to control communicable diseases42 U.S.C. § 264
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Definitions; generally21 U.S.C. § 321