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Congress Requires Dietary Supplement Companies to Report Adverse Reactions to FDA

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Congress Requires Dietary Supplement Companies to Report Adverse Reactions to FDA

Labels to provide consumer information by 2008 WASHINGTON—Within one year, dietary supplement manufacturers will have to list an address or telephone number on product labels that consumers can use to report serious adverse reactions, and companies will have to promptly turn over such information to the Food and Drug Administration (FDA). The new requirement will also apply to over-the-counter drugs


By CSPINET ,US.


Health Policy Resource.