fda
FDA Holds Public Meeting Exploring Scope of Dietary Supplement Ingredients
On March 27, the U.S. Food and Drug Administration (FDA) hosted a public meeting on the scope of dietary supplement ingredients. The event was held in-person from 9 a.m. to 3 p.m. EST at Wiley Auditorium, 5001 Campus Drive in College Park, MD and virtually. FDA’s Office of Dietary Supplement Programs (ODSP) invited stakeholders to ...
Durbin, Blumenthal and Pallone Reintroduce Bill to Prohibit Sale of Tianeptine
On Feb. 5, U.S. Senate Democratic Whip Dick Durbin (D-IL), U.S. Senator Richard Blumenthal (D-CT) and U.S. Representative Frank Pallone (D-NJ) reintroduced the Prohibiting Tianeptine and Other Dangerous Products Act, legislation that would prohibit tianeptine or “gas station heroin” from being marketed to consumers. The law would give the U.S. Food and Drug Administration (FDA) ...
HHS and FDA Take New Approach on “No Artificial Colors” Claims
On Feb. 5, the Department of Health and Human Services (HHS) and U.S. Food and Drug Administration (FDA) announced additional steps to transition the nation’s food supply from the use of artificial petroleum-based colors to alternatives derived from natural sources. In April 2025, HHS and FDA officially announced its plans to phase out petroleum-based synthetic ...
U.S. Representative Introduces Dietary Supplement Regulatory Uniformity Act
On Feb. 4, U.S. Representative Nick Langworthy (R-NY) introduced the Dietary Supplement Regulatory Uniformity Act, legislation aimed at protecting consumer health while restoring common sense to dietary supplement regulation by reaffirming a single, science-based national standard overseen by the U.S. Food and Drug Administration (FDA). According to Langworthy, dietary supplements including vitamins, protein powders, creatine ...
FDA and CDC Investigate Salmonella Contamination in Moringa Leaf Powder
The U.S. Food and Drug Administration (FDA) and the Centers for Disease Control and Prevention (CDC) are investigating a multi-state outbreak of salmonella infections linked to products containing moringa leaf powder. As of Jan. 29, CDC reported a total of 65 people across 28 states have been infected with one of the two outbreak strains ...
Dick Durbin Reintroduces Dietary Supplement Listing Act
On Jan. 15, U.S. Senator Dick Durbin (D-IL) reintroduced the Dietary Supplement Listing Act, which would require dietary supplement manufacturers to register their products with the U.S. Food and Drug Administration (FDA). According to Durbin, the law would require companies to provide FDA with critical information about their products including product names, a list of ...
FDA and DOJ Seize 7-OH Products in Missouri
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 ...
FDA Issues Letter on DSHEA Disclaimer Amendment, Industry Responds
On Dec. 11, the U.S. Food and Drug Administration (FDA) published a letter to the dietary supplement industry regarding the agency’s labeling regulations that govern the placement of the disclaimer on dietary supplements labels under the Federal Food, Drug, and Cosmetic Act (FD&C) and Dietary Supplement Health and Education Act of 1994 (DSHEA). The agency ...
FDA Updates Warnings on “Supplements” Containing Yellow Oleander
On Nov. 3, The U.S. Food and Drug Administration (FDA) completed analytical testing of additional “supplement” products that tested positive for toxic yellow oleander. The analysis determined that certain products labeled as tejocote (Crataegus mexicana) root or Brazil seed were adulterated because they contained yellow oleander (Thevetia peruviana) instead of the labeled ingredients. Yellow oleander ...
Hi-Tech Pharmaceuticals and CEO Convicted of $4.7 Million Wire Fraud Scheme
Dietary supplement company Hi-Tech Pharmaceuticals, Inc. and its CEO, Jared Wheat, were convicted by a federal jury of wire fraud after “fabricating documents to deceive customers into believing that the company was certified as compliant with industry manufacturing standards.” In 2007, the U.S. Food and Drug Administration (FDA) issued new mandatory guidelines on sanitary, hygienic ...
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