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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 F - Biologics |
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Part 606 - Current Good Manufacturing Practice for Blood and Blood Components |
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Subpart G - Additional Labeling Standards for Blood and Blood Components |
| § 606.120 - Labeling, general requirements. |
| § 606.121 - Container label. |
| § 606.122 - Circular of information. |