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Durbin, Braun Introduce Legislation to Mandate Product Listings for Dietary Supplements

by Shari Barbanel | May 4, 2022

U.S. Senate Majority Whip Dick Durbin (D-IL) and U.S. Senator Mike Braun (R-IN) introduced the Dietary Supplement Listing Act of 2022, bipartisan legislation to require dietary supplement manufacturers to list their products with the U.S. Food and Drug Administration (FDA). The Dietary Supplement Listing Act of 2022 would require companies to provide FDA with vital information about their ...

NPA Launches Warning Letter Database for Member Companies

by Shari Barbanel | August 5, 2016

The Natural Products Association (NPA) has announced the launch of its highly anticipated warning letter database. This database will be a free online tool for NPA members to view violations against the dietary supplement good manufacturing practices (GMPs), which are deemed as ‘technical adulterations’ by the FDA (U.S. Food and Drug Administration), dietary supplement labeling ...

NPA Sends Letter to New FDA Commissioner

by Shari Barbanel | March 2, 2016

The Natural Products Association (NPA) sent a letter to Dr. Robert Califf regarding his recent confirmation to become the new commissioner of the U.S. Food and Drug Administration (FDA).  In the letter, NPA congratulated Califf on his confirmation by the U.S. Senate and outlined its priorities for the new commissioner.  NPA also requested a meeting ...

DOJ Announces Supplement Sweep – CRN, NPA and AHPA Express Support

by Shari Barbanel | November 18, 2015

On Tuesday, November 17, Ben Mizer,  principal deputy assistant attorney general for the Civil Division of the Department of Justice (DOJ), revealed the government’s plan for a sweep of actions targeting unlawful dietary supplement makers and marketers. “We are here today to explain the critical steps the federal government is taking to stem the tide ...

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