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  1. LII
  2. Electronic Code of Federal Regulations (e-CFR)
  3. Title 21. Food and Drugs
  4. Chapter I. FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES
  5. Subchapter B. FOOD FOR HUMAN CONSUMPTION
  6. Part 111. CURRENT GOOD MANUFACTURING PRACTICE IN MANUFACTURING, PACKAGING, LABELING, OR HOLDING OPERATIONS FOR DIETARY SUPPLEMENTS
  7. Subpart G. Production and Process Control System: Requirements for Components, Packaging, and Labels and for Product That You Receive for Packaging or Labeling as a Dietary Supplement

21 CFR Subpart G - Production and Process Control System: Requirements for Components, Packaging, and Labels and for Product That You Receive for Packaging or Labeling as a Dietary Supplement

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  1. § 111.153 What are the requirements under this subpart G for written procedures?
  2. § 111.155 What requirements apply to components of dietary supplements?
  3. § 111.160 What requirements apply to packaging and labels received?
  4. § 111.165 What requirements apply to a product received for packaging or labeling as a dietary supplement (and for distribution rather than for return to the supplier)?
  5. § 111.170 What requirements apply to rejected components, packaging, and labels, and to rejected products that are received for packaging or labeling as a dietary supplement?
  6. § 111.180 Under this subpart G, what records must you make and keep?

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