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Code of Federal Regulations (Last Updated: November 8, 2024) |
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Title 21 - Food and Drugs |
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Chapter I - Food and Drug Administration, Department of Health and Human Services |
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SubChapter B - Food for Human Consumption |
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Part 111 - Current Good Manufacturing Practice in Manufacturing, Packaging, Labeling, or Holding Operations for Dietary Supplements |
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Subpart M - Holding and Distributing |
| § 111.453 - What are the requirements under this subpart for M written procedures? |
| § 111.455 - What requirements apply to holding components, dietary supplements, packaging, and labels? |
| § 111.460 - What requirements apply to holding in-process material? |
| § 111.465 - What requirements apply to holding reserve samples of dietary supplements? |
| § 111.470 - What requirements apply to distributing dietary supplements? |
| § 111.475 - Under this subpart M, what records must you make and keep? |