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Business · 04/08/2009Updated: 10/17/2026 · 1 min read

FDA Announces Approval of Dietary Supplement Data Collection Under Paperwork Reduction Act

Summary

The Food and Drug Administration (FDA) has announced that it has received approval from the Office of Management and Budget (OMB) to collect information on adverse events and recordkeeping for dietary supplements, as mandated by the Dietary Supplement and Nonprescription Drug Consumer Protection Act of 1995.

Original source language: Federal Register — Food and Drug AdministrationOpen original release →

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