Kyle Diamantas
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 ...
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 ...
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 ...
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