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FDA Commissioner Dr. Marty Makary Resigns

by Shari Barbanel | May 13, 2026

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 ...

India Bans Ashwagandha Leaves in Supplements, Industry Responds

by Shari Barbanel | May 4, 2026

On April 16, India’s regulatory agency, Food Safety and Standards Authority of India (FSSAI), banned products containing ashwagandha leaves, stating only ashwagandha roots and their extracts are permitted for use in health supplements, nutraceuticals and certain food products as per government regulations. “It has been brought to the notice of FSSAI that certain manufacturers of these products ...

Industry Responds to Introduction of New Dietary Supplement Listing Act

by Shari Barbanel | April 29, 2026

On April 20, U.S. Representative Maxine Dexter, MD (D-OR) introduced a new Dietary Supplement Listing Act to require dietary supplement manufacturers to register their products with the U.S. Food and Drug Administration (FDA). A similar bill was introduced in 2024 and then reintroduced in 2026 by Senator Dick Durbin (D-IL). The Dietary Supplement Listing Act ...

Supreme Court Finds Trump’s Tariffs Unlawful; Refund and New Questions Remain

by Shari Barbanel | February 23, 2026

On Feb. 20, the United States Supreme Court ruled in the consolidated case Learning Resources, Inc. v. Trump that the International Emergency Economic Powers Act (IEEPA) does not grant the President of the United States the authority to impose tariffs. This ruling found that almost all of the major tariffs implemented by the current administration were unlawful, including ...

U.S. Representative Introduces Dietary Supplement Regulatory Uniformity Act

by Shari Barbanel | February 18, 2026

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 ...

Expo West Celebrates 45 Years, Plans Biggest Show to Date

by Shari Barbanel | February 16, 2026

Natural Products Expo West returns to the Anaheim Convention Center in Anaheim, CA from March 3-6. According to show organizers, 2026 is a milestone year as Expo West celebrates 45 years with the biggest show to date. The new CPG Innovation Summit is a one-day immersive experience built to connect brands with the resources they ...

Dick Durbin Reintroduces Dietary Supplement Listing Act

by Shari Barbanel | January 19, 2026

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 Issues Letter on DSHEA Disclaimer Amendment, Industry Responds

by Shari Barbanel | December 15, 2025

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 ...

Tariff Relief Expanded for Certain Botanical Ingredients

by Shari Barbanel | November 24, 2025

As part of an executive order issued on Nov. 14, President Donald Trump revised and expanded the set of commodities in the Harmonized Tariff Schedule (HTS) that are exempt from reciprocal tariffs. These changes, which are reflected in updates to Annex II and Annex III partially target commodities that cannot be sourced within the United States. According ...

AHPA Launches New Technology & AI Innovation Committee

by Shari Barbanel | October 6, 2025

The American Herbal Products Association (AHPA) has announced the formation of its new Technology & AI Innovation Committee to help members explore opportunities, navigate challenges, and apply best practices in the rapidly evolving fields of artificial intelligence (AI) and related technologies. The committee will be chaired by Asa Waldstein, founder & principal of Apex Compliance, who ...

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