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FDA cosmetic adverse reaction reporting program eliminated -- Federal Register proposal.

This article was originally published in The Rose Sheet

Executive Summary

FDA COSMETICS ADVERSE REACTION "COMPREHENSIVE REVIEW" TO BE COMPLETED BY SEPT. 30, the end of FDA's fiscal year, the agency said. The review will use FDA's cosmetics adverse reactions database, which consists of 10-12 years of industry submissions gathered through the Voluntary Cosmetic Reporting Program (VCRP), to analyze adverse reaction trends across product categories and subcategories and to calculate baseline rates of adverse events.
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