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FDA and DOJ Seize 7-OH Products in Missouri

by Eric Munson | January 5, 2026

In December 2025, the U.S Food and Drug Administration (FDA) and the U.S. Department of Justice (DOJ) seized approximately 73,000 units of 7-hydroxymitragynine (7-OH) products—valued at about $1 million—from three firms in Missouri. The seizure focused on foods and dietary supplements products—including liquid shots and tablets—that contain 7-OH as an ingredient. Concentrated 7-OH has been ...

CRN Calls Out New York Supplement Law in DOJ Filing

by Eric Munson | September 22, 2025

On Sept. 15, the Council for Responsible Nutrition (CRN) submitted a new filing to the Department of Justice (DOJ) regarding the New York State supplement law. On Oct. 25, 2023, New York Governor Kathy Hochul signed Assembly Bill A5610-D/Senate Bill S5823-C, banning the sale of weight-loss and sports nutrition supplements to minors. In its filing, ...

DOJ Asks Court to Dismiss Lawsuit Against Xlear

by Eric Munson | March 17, 2025

On March 10, the Department of Justice (DOJ) asked the United States District Court of Utah to dismiss the Federal Trade Commission (FTC)’s lawsuit against Xlear (American Fork, UT) and its CEO Nathan Jones. In October 2021, FTC filed a lawsuit against Xlear and Jones alleging the company’s statements that its nasal spray could serve ...

NPA Launches Warning Letter Database for Member Companies

by Nicholas Saraceno | August 5, 2016

The Natural Products Association (NPA), the largest trade association for the dietary supplement industry, is announcing 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 ...

NPA Sends Letter to New FDA Commissioner

by Corinne Anderson | February 29, 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 ...

US Marshals Seize Dietary Supplements Containing Kratom

by Corinne Anderson | February 8, 2016

The U.S. Food and Drug Administration (FDA) announced that U.S. Marshals, at the agency’s request, seized nearly 90,000 bottles of dietary supplements labeled as containing kratom. The product, manufactured for and held by Dordoniz Natural Products LLC, located in South Beloit, IL, is marketed under the brand name RelaKzpro and worth more than $400,000. “We ...

NPA Seeks FDA Nominee’s Position on Supplement Regulation

by Corinne Anderson | November 30, 2015

The Natural Products Association (NPA) submitted a letter to U.S. Senate Health, Education, Labor and Pensions Committee Chairman Lamar Alexander and Ranking Member Patty Murray requesting the president’s nominee to lead the Food and Drug Administration (FDA) clarify past comments related to the regulation of the supplement industry. Dr. Robert Califf, in a November 2010 ...

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

by Corinne Anderson | November 18, 2015

On Tuesday, Nov. 17, Ben Mizer,  principal deputy assistant attorney general for the Civil Division of the 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 of unlawful dietary ...

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