
ParActin Andrographis paniculata from HP Ingredients, was granted a product license (#80109555) from Health Canada to support joint health symptoms.

ParActin Andrographis paniculata from HP Ingredients, was granted a product license (#80109555) from Health Canada to support joint health symptoms.

The Council for Responsible Nutrition is calling on Congress to address an unintended “loophole” in the Food, Drug, and Cosmetic Act (FD&C Act) that casts doubt on the legal authority of the U.S. Food and Drug Administration (FDA) to regulate products that do not mee the strict definition of “dietary supplement” in the statute.

What are the biggest problems in the dietary supplements market, and will changing DSHEA fix them?

The act was created to protect financial institutions providing financial services to cannabis-related legitimate businesses and service providers.

Last week, California’s Assembly Health Committee voted to ban sales of weight-loss dietary supplements to minors. The bill is headed for another round of votes and could ultimately be signed into law.

Bio-Cat Microbials LLC has received a “Letter of No Objection” from the U.S. Food and Drug Administration (FDA) regarding the company’s GRAS (generally recognized as safe) notice for its Opti-Biome Bacillus subtilis MB40 probiotic.

Verdure Sciences launched Longvida, a turmeric extract standardized to curcumin and total curcuminoids (solid lipid curcumin particle - SLCP), in Brazil after receiving ANVISA approval through distribution partner Kilyos Nutrition

National and state efforts could expand or restrict access to a number of dietary supplement products.

CV Sciences, Inc. formed an ongoing partnership with Alkemist Labs to collaborate with the National Institute of Standards and Technology (NIST) on efforts to help cannabis testing labs demonstrate and improve measurement capabilities and comparability.

Vidya Herbs Inc. recently announced it achieved self-affirmed Generally Recognized as Safe (GRAS) designation for its green coffee extract, CGA-7.

Deerland Probiotics & Enzymes attained a list of published health claims following the inclusion of its DE111 probiotic as a food ingredient under the Food Standards Australia New Zealand (FSANZ) Code.

There’s renewed interest in respiratory-support ingredients. What’s in the toolbox, and do they work?

Preliminary findings show no evidence of liver disease in the 839 participants and no increase in the prevalence of elevated liver function tests.

Earlier this month, Folium Biosciences submitted a novel food application to the UK Food Standards Agency (FSA) for validation of its hemp-derived, 0.0% THC broad-spectrum cannabidiol (CBD) oil.

For leading medical nutrition companies, South Asia is a prime market for expansion.

The European Industrial Hemp Association’s (EIHA) Novel Food Consortium has received confirmation from the UK Food Standards Agency (FSA) that its novel foods application has been approved and its members’ CBD products can remain on UK shelves.

A recent study conducted by NSF International and Harvard Medical School found nine prohibited stimulants in 17 sports and weight loss supplements on top of the illegal Deterenol already on the label.

E-commerce has seen explosive growth since the COVID-19 pandemic started. Here’s how social media skills will influence sales in 2021.

FDA explained in its warning letters to the firms that even if CBD in the product was labeled as an inactive ingredient, the product cannot be legally marketed without an approved new drug application.

Curcugen, a bioavailability-enhanced, water-dispersible curcuminoid complex from DolCas Biotech has achieved self-affirmed GRAS (generally recognized as safe) status.

Xavier Becerra, the former attorney general of California, has been narrowly confirmed as the new secretary for the Department of Health and Human Services by a vote of 50 to 49.

The Global Retail and Manufacturing Alliance (GRMA) announced the successful completion of the ANSI National Accreditation Board (ANAB) pilot accreditation program.

The FDA import alert, issued to two foreign companies over stimulant ingredient higenamine, could have widescale repercussions in the dietary supplements industry by finally getting more firms to file New Dietary Ingredient notifications.

Bestevia Rebaudioside B from SweeGen (Rancho Santa Margarita, CA) received a GRAS (generally recognized as safe) no objection letter from FDA.

Gencor announced that AGEprost is listed on Health Canada’s Licensed Natural Health Products Database (LNHPD) for prostate health claims.

The Natural Products Association recently testified at a public hearing before California’s Senate Committee on Health on new legislation the state is considering that would establish standards for CBD products, and prevent manufacturers as well as distributors from making false claims.

ABC-AHP-NCNPR Botanical Adulterant Prevention Program (BAPP) is celebrating 10 years of research and educational activities. The program was founded by the American Botanical Council (ABC) in 2011 in partnership with consortium members.

The European Industrial Hemp Association’s Novel Food Consortium has submitted its Novel Foods application to the UK Food Standards Authority (FSA) ahead of the March 31, 2021 deadline.

The 5-part program will dive deep into cultivation, extraction, processing, testing, third-party certifications, and more.

Pharmako Biotechnologies, the sister company of Gencor in the U.S., received approval from the Therapeutic Goods Administration (TGA), Department of Health and Aging for the Government of Australia, for its manufacturing facility.