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Proposed H.R. 10336 Would Balance Innovation, Access to Dietary Supplements—Yet Change the Definition

On September 10, 2026, Congresswoman Diana Harshbarger (R-TN) introduced H.R. 10336—the Dietary Supplement Innovation Act—which would modernize the U.S. Food and Drug Administratio...

Trade Associations Applaud Dietary Supplement Innovation Act

On Sept. 10, Congresswoman Diana Harshbarger (R-TN) introduced the Dietary Supplement Innovation Act, legislation that is designed to modernize the Food and Drug Administration’s d...

Dietary Supplement Innovation Act Aims to Address Drug Preclusion Concerns

Representative Diana Harshbarger (R-TN) recently introduced the Dietary Supplement Innovation Act (H.R. 10336), legislation that would amend the Federal Food, Drug, and Cosmetic Ac...

CRN Celebrates Dietary Supplement Exemption on California Food Date Label Law

The Council for Responsible Nutrition (CRN) is celebrating a significant state advocacy victory following enactment of California Assembly Bill 2779 (AB 2779), which excludes dieta...

Australia Restricts Herbal Supplement Over Anaphylaxis Risk While It Remains Available in US

Australia is removing Andrographis medicines over anaphylaxis concerns while the herbal ingredient remains widely available in US dietary supplements. The post Australia Restricts...

HHS Recommends Thresholds to Target Synthetic, Concentrated 7-OH Products

The U.S. Department of Health and Human Services (HHS) provided new recommendations to the Drug Enforcement Administration (DEA) that establish science-based thresholds for 7-hydox...

CRN Survey Shows Consumer Support for Federal Dietary Supplement Listings

The Council for Responsible Nutrition (CRN) released findings from its 2026 national consumer survey, which adds consumer perspective to its longstanding support for a federal diet...

FSSAI directs nutraceutical makers to ensure mandatory warning statements on products with herbal extracts

The regulator has asked nutraceuticals and health supplements makers to review their product labels to ensure compliance as violations will attract stringent action including susp...

California Advances New Menu Disclosure Requirements and Excludes Supplements from Date Labeling Law

FBOs asked to display botanical parts on product labels

The Food Safety and Standards Authority of India FSSAI has issued an advisory making it mandatory for manufacturers of health supplements nutraceuticals and special dietary foods t...

Supplement Marketing Claims: FDA and FTC Rules Explained

Supplement marketing claims need an FDA notification within 30 days and FTC-grade human trial evidence. See what each rule requires before you publish.

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...

U.S. Supreme Court Declines to Review New York Age Restriction Law

The Council for Responsible Nutrition (CRN) expressed “disappointment” that the U.S. Supreme Court declined to review CRN’s challenge to a New York law restricting the sale of cert...

FDA Finalizes NDIN Identity and Safety Guidance

FDA Recalls RAPTURE Pre-Workout After Detecting DMAA: Scientific Analysis of the Controversial Stimulant

The nationwide recall of a DMAA-containing pre-workout supplement raises renewed questions about stimulant pharmacology, cardiovascular safety, ingredient testing, and federal regu...

As Weight-Loss Drug Users Turn To Dietary Supplements, Doctors, Regulators Raise Flags

Rising supplement use among GLP-1 users is boosting sales, while doctors warn about safety risks and US regulators consider tighter oversight.