CFR section
21 CFR 111.420(a): What requirements apply to repackaging and relabeling?
PART 111-CURRENT GOOD MANUFACTURING PRACTICE IN MANUFACTURING, PACKAGING, LABELING, OR HOLDING OPERATIONS FOR DIETARY SUPPLEMENTS · Subpart L-Production and Process Control System: Requirements for Packaging and Labeling Operations
Key facts
| Citation | 21 CFR 111.420(a) |
|---|---|
| Section | What requirements apply to repackaging and relabeling? |
| Part | PART 111-CURRENT GOOD MANUFACTURING PRACTICE IN MANUFACTURING, PACKAGING, LABELING, OR HOLDING OPERATIONS FOR DIETARY SUPPLEMENTS |
| Subpart | Subpart L-Production and Process Control System: Requirements for Packaging and Labeling Operations |
| Subchapter | 21 CFR B Food |
| Product types cited | Food/Cosmetics |
| Regulation text (excerpt) | (a) You may repackage or relabel dietary supplements only after quality control personnel have approved such repackaging or relabeling. |
At a glance
- 1–9 Inspections citing this section
- 1–9 Warning letters citing this section
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About CFR sections cited by the FDA
Title 21 of the Code of Federal Regulations contains the FDA's regulations, including current good manufacturing practice and quality system requirements that inspections cite.