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Code of Federal Regulations (Last Updated: July 5, 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 A - General Provisions |
§ 111.1 - Who is subject to this part? |
§ 111.3 - What definitions apply to this part? |
§ 111.5 - Do other statutory provisions and regulations apply? |