---
kind: "section"
citation: "21 C.F.R. § 111.120"
title: "21"
number: "111.120"
heading: "What quality control operations are required for components, packaging, and labels before use in the manufacture of a dietary supplement?"
url: "https://uscodex.org/cfr/21/111.120"
---

# §111.120. What quality control operations are required for components, packaging, and labels before use in the manufacture of a dietary supplement?


Quality control operations for components, packaging, and labels before use in the manufacture of a dietary supplement must include:

- (a) Reviewing all receiving records for components, packaging, and labels;
- (b) Determining whether all components, packaging, and labels conform to specifications established under § [111.70 (b)](/cfr/21/111.70.md?p=b) and [(d)](/cfr/21/111.70.md?p=d);
- (c) Conducting any required material review and making any required disposition decision;
- (d) Approving or rejecting any treatment and in-process adjustments of components, packaging, or labels to make them suitable for use in the manufacture of a dietary supplement; and
- (e) **Approving, and releasing from quarantine, all components, packaging, and labels before they are used.**

## 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.