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DSHEA


Dick Durbin Reintroduces Dietary Supplement Listing Act

by Eric Munson | 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 Eric Munson | 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 ...

CHPA Survey Shows Strong Support for Dietary Supplement Reform

by Eric Munson | June 9, 2025

On June 3, the Consumer Healthcare Products Association (CHPA) released the results of a new survey* which shows widespread consumer use and value in dietary supplements, and strong support for modernizing federal regulations. According to the survey, 92 percent of consumers agree supplements had a positive impact on their overall health, wellness and quality of ...

Oregon Introduces Cannabinoid Safety and Regulation Act to Protect Children

by Eric Munson | October 7, 2024

United States Senator Ron Wyden (D-OR) introduced the Cannabinoid Safety and Regulation Act (CSRA) to establish national standards to protect public health and safety and keep cannabis products out of the hands of children. The bill is co-sponsored by Senator Jeff Merkley (D-OR). According to Wyden, the CSRA would establish a national age restriction to ...

NPA Files Lawsuit Against FDA’s “Unlawful Application” of Food, Drug and Cosmetic Act

by Eric Munson | August 30, 2024

The Natural Products Association (NPA) filed a lawsuit on August 28 against the U.S. Food and Drug Administration (FDA), requesting the agency cease its “unlawful retroactive application” of the Food, Drug and Cosmetic Act against nicotinamide mononucleotide (NMN). “We are extremely grateful for the leadership shown by our organization’s members in deciding to take this ...

Super Natural Health Food Center

by Eric Munson | July 1, 2024

50 Years of Supplements in a Small Missouri City Since 1973, Super Natural Health Food Center has existed at the same location in Grandview, MO, a small city about 16 miles south of Kansas City. After more than 50 years, Owner Joseph D. Tittone continues to dutifully serve and educate his customers. Tittone’s wife, Kelly ...

30 People Who Shaped the Natural Products Industry

by James Gormley | January 3, 2024

In commemoration of Vitamin Retailer magazine’s 30th anniversary, we assembled a list of 30 people who shaped, built and defended the natural products industry over the last 30 years. The year 2024 is also the 30th anniversary of the enactment of the Dietary Supplement Health and Education Act (DSHEA) of 1994. For every person we ...

Trade Associations Respond to Congressional Request for Information on CBD

by Angela Sabarese | August 18, 2023

The Council for Responsible Nutrition (CRN) and the Natural Products Association (NPA) have submitted responses to a Congressional Request for Information (RFI) seeking insight from industry stakeholders on CBD in order to develop “a regulatory pathway for non-intoxicating hemp-derived cannabinoid products that prioritizes consumer safety and provides certainty to the U.S. markets.” According to CRN, ...

AHPA Announces Release of Herbs of Commerce, Third Edition

by Angela Sabarese | July 17, 2023

The American Herbal Products Association (AHPA) has announced the release of the third edition of Herbs of Commerce. The publication provides guidance on the consistent naming of botanical ingredients on product labels, especially those marketed in the U.S. as dietary supplements, according to the association. It is now available for purchase on Amazon. AHPA published ...

CRN Submits Citizen Petition Requesting FDA to Re-interpret Drug Preclusion Clause

by Angela Sabarese | May 16, 2023

The Council for Responsible Nutrition (CRN) has submitted a Citizen Petition to the FDA requesting that the agency to reconsider its interpretation of the Drug Preclusion Clause. According to the Washington, DC-based trade association, the Clause has been, and will likely continue to be, misapplied to dietary supplement ingredients that FDA has previously acknowledged as ...

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