CLEAR LABELS Act
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Summary
The CLEAR LABELS Act amends the Federal Food, Drug, and Cosmetic Act to require drug manufacturers to include on labels the name, place of business, and facility identifier of the original manufacturer of active pharmaceutical ingredients and finished drug products, as well as packers and distributors. This information may be provided directly on the label or through electronic means such as QR codes or searchable portals. The bill also exempts finished drug products that comply with these new labeling requirements from federal customs country-of-origin marking rules.
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