CHPA
California Passes Age Restriction Law on Weight-loss and Muscle-building Supplements
On Sept. 28, California Governor Gavin Newsom signed Assembly Bill 2030, which prohibits the sale of certain dietary supplements to consumers under the age of 18. AB 2030 prohibits the sale of dietary supplements that are “labeled, marketed or otherwise represented for weight loss or muscle building,” and over-the-counter diet pills to consumers under 18 (with ...
CHPA Honors Julie Aker with 2026 William Cooley Career Achievement Award
The Consumer Healthcare Products Association (CHPA) has announced that Julie Aker, former chief executive officer of Concentrics Research, is this year’s recipient of the William Cooley Regulatory & Scientific Affairs Career Achievement Award, recognizing a career defined by scientific innovation, regulatory leadership, and extraordinary contributions to advancing Rx-to-OTC (over-the-counter) switches and consumer access to self-care. Named ...
CHPA President & CEO Scott Melville Announces Plans for Leadership Transition
The Consumer Healthcare Products Association (CHPA) has announced that President and CEO Scott Melville will step down from his role early next year following 16 years of leadership. Since becoming president and CEO in 2010, Melville has led a period of significant growth and transformation for CHPA, expanding the association from its traditional focus on ...
Trump Nominates Dr. Heidi Overton as FDA Commissioner
President Donald Trump announced his nomination of Heidi Overton, MD, PhD as the commissioner for the U.S. Food and Drug Administration (FDA). Overton would replace Dr. Marty Makary who resigned in May 2026. Kyle Diamantas, JD, has been serving as acting commissioner. Overton is a physician and health care policy leader currently served as deputy assistant to ...
Associations Respond to Mandatory GRAS Notification Proposal
The U.S. Department of Health and Human Services (HHS) and U.S. Food and Drug Administration (FDA) proposed a rule requiring manufacturers to notify FDA whenever they conclude the use of a substance added to human or animal food is generally recognized as safe (GRAS). Since Congress established the GRAS exemption in 1958, manufacturers have been ...
Senators Introduce Dietary Supplements Access Act, Industry Responds
On May 20, U.S. Senators Kevin Cramer (R-ND) and John Curtis (R-UT) introduced the Dietary Supplements Access Act, legislation that would allow dietary supplements to be purchased using HSAs (Health Savings Accounts), FSAs (Flexible Spending Accounts), and HRAs (Health Reimbursement Arrangements). The measure is designed to give families more flexibility to invest in preventative health solutions ...
FDA Commissioner Dr. Marty Makary Resigns
On May 12, U.S. Food and Drug Administration (FDA) Commissioner Dr. Marty Makary resigned from his position after 13 months. As reported by The New York Times, he faced mounting pressure and criticism, ultimately leaving over the Trump administration’s plans to authorize fruit-flavored e-cigarettes and vapes. Makary is a surgical oncologist, professor, researcher, author and medical ...
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 Dr. in College Park, MD and virtually. FDA’s Office of Dietary Supplement Programs (ODSP) invited stakeholders to participate in ...
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 ...
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 ...
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