Regulatory

U.S. Senate Majority Whip Dick Durbin (D-IL), introduced the Dietary Supplement Listing Act of 2022 on Tuesday. The bipartisan legislation, co-sponsored by Senator Mike Braun (R-IN), would require dietary supplement manufacturers to list their products with the U.S. Food and Drug Administration.

The draft guidance sets in motion FDA’s policy of enforcement discretion while the agency reviews NAC’s safety.

One expert explains why sustainability and food safety go hand in hand.

The annual Legal, Regulatory & Compliance Forum on Dietary Supplements will take place in person on June 29-30 at the Westin Grand Central hotel in New York City.

Canyon Labs opened a 17,000 square foot, full-service lab in Salt Lake City that offers testing, scientific and technical consulting, and Institutional Review Board (IRB) clinical services.

The GRAS status of these strains completes the portfolio of 19 strains of quadruple-coated probiotics offered by Nutralliance, available in single-strain solutions and custom blends.

The UK's Food Standards Agency’s published a list of cannabinoid products that are permitted for sale to consumers—only these products are authorized for sale. Full authorization is expected in 2023.

Industry associations discuss with Nutritional Outlook what their next steps could be.

Ingredients by Nature announced the self-affirmed GRAS (generally recognized as safe) status of Eriomin, a high potency standardized extract of lemon-based flavonoids.

Three human clinical studies show that the ingredient can help manage symptoms related to upper respiratory challenges and can help positively modulate immune responses, the company says.

The world of natural products for smokers’ health is complex and perilous. Can dietary supplements succeed in this market?

A recent budget request submitted by the U.S. Food and Drug Administration for Fiscal Year 2023 states that requested funds could help support the establishing of a “product listing requirement.”

On February 22, 2022, a new regulation kicked into effect in the EU for infant formulas and follow-on formulas containing protein hydrolysates, requiring companies to submit dossiers on their ingredients so that EFSA can evaluate their safety and suitability for use in these products.

The bill specifically restricts dietary supplements containing an ephedrine group alkaloid, and any supplement containing: androstanedoil, androstenedione, androstenedione, noradrostenediol, noradrostenediol, and dehydroepiandrosterone.

BeVeg is the only ISO 17065–accredited program and vegan trademark.

Methyloxolane is a bio-based solvent for the extraction of vegetable oils, plant proteins, and other natural ingredients that is produced from agricultural by-products such as sugarcane bagasse.

Sweegen announced that its entire Signature Bestevia portfolio is now accessible to brands in Mexico after the country’s safety authority adopted the Codex Alimentarius (Codex) specifications for steviol glycosides produced by different technologies.

Welch has been acting director of ODSP since Steve Tave left the position in March of 2021.

The health claim recognizes the strain’s ability to support healthy bowel habits in adults with irritable bowel syndrome (IBS) at a daily dose of 10 billion colony-forming units (CFU).

FDA finally has a commissioner at the helm again. But can the dietary supplements industry expect that new FDA Commissioner Robert Califf will prioritize reforming and strengthening dietary supplement regulations—a lofty goal FDA’s leadership first set in 2019?

The Natural Products Association announced that Douglas Kalman, PhD, RD, will join the organization as its new senior vice president of scientific and regulatory affairs.

The company’s portfolio includes its Gummiceuticals line of sugar-free, vegan gummy supplements introduced last year.

No doubt diet plays a part in the rise and fall of blood sugar, so is there a place for dietary ingredients in helping consumers manage their blood sugar?

The GRAS notice was submitted by GRAS Associates, a fully owned subsidiary of Nutrasource, on behalf of Howtian.

The citizen's petition requests FDA to stop excluding hemp-derived CBD from the definition of a dietary supplement, and includes an NDIN from cbdMD, which the petition asks FDA to substantively review, unlike previous NDINs.

A recent Op-Ed expressed concern about the impact dietary supplement usage in the armed forces could have on military readiness.

Nutrasource’s IGEN non-GMO third-party certification program verifies non-GMO label claims for dietary supplements and food.

Notably, said Sabinsa in a press release, “This may well be the first time a metabolite of a nutrient has been approved as a Novel Food.”

Two strains are Lactobacillus rhamnosus 19070-2 and Lactobacillus reuteri 12246-CU.

Earthlight, a whole-food vitamin D ingredient provided by PLT Health Solutions, has gained approval from ANVISA, allowing its use as an ingredient in food, beverages, and dietary supplements sold in Brazil.