CFR section
21 CFR 111.415(e): What requirements apply to filling, assembling, packaging, labeling, and related operations?
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 111.415(e) |
|---|---|
| Section | What requirements apply to filling, assembling, packaging, labeling, and related operations? |
| 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 | Drugs, Food/Cosmetics |
| Regulation text (excerpt) | (e) Identifying, by any effective means, filled dietary supplement containers that are set aside and held in unlabeled condition for future label operations, to prevent mixups; |
At a glance
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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.