---
kind: "section"
citation: "21 C.F.R. § 111.420"
title: "21"
number: "111.420"
heading: "What requirements apply to repackaging and relabeling?"
url: "https://uscodex.org/cfr/21/111.420"
---

# §111.420. What requirements apply to repackaging and relabeling?

- (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)](/cfr/21/111.70.md?p=g).
- (c) Quality control personnel must approve or reject each batch of repackaged or relabeled dietary supplement prior to its release for distribution.

## Notes

### Authority

Authority: 21 U.S.C. 321, 342, 343, 371, 374, 381, 393; 42 U.S.C. 264.

### Source

Source: 72 FR 34942, June 25, 2007, unless otherwise noted.