Code of Federal Regulations (Last Updated: July 5, 2024) |
Title 21 - Food and Drugs |
Chapter I - Food and Drug Administration, Department of Health and Human Services |
SubChapter B - Food for Human Consumption |
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 |
Subpart L - Production and Process Control System: Requirements for Packaging and Labeling Operations
§ 111.403 - What are the requirements under this subpart L for written procedures? |
§ 111.410 - What requirements apply to packaging and labels? |
§ 111.415 - What requirements apply to filling, assembling, packaging, labeling, and related operations? |
§ 111.420 - What requirements apply to repackaging and relabeling? |
§ 111.425 - What requirements apply to a packaged and labeled dietary supplement that is rejected for distribution? |
§ 111.430 - Under this subpart L, what records must you make and keep? |