The Federal Trade Commission has handed down the another substantial penalty this year for a misleading Made in USA claim, underlining the risk such claims can pose to manufacturers if not properly constituted
A group of researchers from Taiwan has cautioned against the use of certain Chinese herbal medicines by athletes, stating that it could increase the production of red blood cells and potentially violate doping regulations.
Vitamin B6 supplement dosages should be restricted to 10 mg/day or less, with higher dosages sold only as prescriptions, a citizen petition to FDA has requested. Industry stakeholders say the action is unwarranted and ignores already established safe...
California Gov. Gavin Newsom has signed a bill into law making hemp/CBD supplements and foods legal after an unsettled period in which the state health department was following a federal lead in ruling that CBD was not a legal dietary ingredient.
A recent survey by the American Herbal Products Association showed that over 50% of its members oppose a mandatory product listing for dietary supplements, with only 18% supporting the listing.
The attorney is one of the most well-known and respected lawyers in the dietary supplement scene and has become a nationally recognized thought leader on the regulation of CBD and other hemp products, as well as many other regulatory issues facing the...
After five years of litigation, jurors in federal district court in California delivered a split verdict in the years long legal dispute between ChromaDex and Elysium, with both sides claiming victory.
FDA has issued a warning letter to dietary supplement manufacturer that is based in part on the presence of the problematical ingredient higenamine in some of the company’s products.
The Federal Trade Commission has issued a policy mandating that companies using health apps and wearable connected devices must comply with a rule governing how consumers must be informed if a data breach occurs.
US Judge Colm Connolly, United States District Court for the District of Delaware, has granted the request from Elysium Health to invalidate two Dartmouth College patents licensed by ChromaDex relating to nicotinamide riboside.
A research team led by prominent industry critic Dr Pieter Cohen has found that FDA warning letters sent to companies using phenibut in dietary supplements didn’t prevent other firms from continuing to use the illegal ingredient.
The ongoing inaction by the US Food and Drug Administration over CBD (cannabidiol) in foods and dietary supplements is having a negative impact on trademark laws, says an industry lawyer.
A new Congressional report on dietary supplements reflects recent priorities with a heavy emphasis on a proposed mandatory product registry and the CBD question.
New research has warned about the importance of expert guidance and biochemical monitoring for sports nutrition users, as it finds a link between supplement consumption and alterations in liver and kidney function.
The American Herbal Products Association has announced a focus on immunity for its annual Congress event that traditionally is scheduled to follow on the Supply Side West trade show in Las Vegas.
US federal regulatory agencies have issued warnings on the availability of delta-8 THC, saying reports of almost 150 recent emergency room visits have mentioned the substance.
An FDA warning letter has been issued for a an under the radar topical herbal product known as Black Salve that continues to appear on the market even after the Agency issued a consumer warning calling the product “life threatening.”
The US Food and Drug Administration has announced 12 winners of a challenge aimed at increasing supply chain transparency and traceability for ingredients and whole foods.
The California Legislature has passed a bipartisan bill to establish rules for the production and marketing of CBD/hemp products. Proponents expect Gov. Gavin Newsom to sign the bill into law before the Oct. 10 deadline.
A bill has been introduced into the US House of Representatives that would allow Health Savings Account (HSA) funds to be used to pay for dietary supplements. The bill mirrors most of the provisions of a bill already in the Senate.
By Daniel Fabricant, PhD, Natural Products Association
NPA president and CEO Daniel Fabricant, PhD, argues that FDA does not need new authorities to regulate the CBD market and that determining a safe daily intake level for the substance should be an integral part of that process.
A company that develops synthetic glycans as targeted microbiome therapies has received an FDA warning letter over the way it has conducted two clinical trials.
Despite being a multi-billion dollar industry, there are no graduate degree programs from accredited academic institutions for executives in the nutrition business sector—until now. The Southwest College of Naturopathic Medicine & Health Sciences...
A-Mansia Biotech’s pasteurised Akkermansia muciniphila is the first next generation gut microbe to get the green light from EFSA, opening the door to a "new generation of nutritional supplements".
Amazon heightened the priority of ISO/IEC 17025:2017 when it announced to dietary supplement sellers that ISO accreditation is required, along with Current Good Manufacturing Practice (CGMP) in order to sell products on its online retail platform.
Branded ingredient firm AIDP has achieved Health Canada registration for a prebiotic beauty-from-within offering. The approval will help the company capitalize on a wave of interest in such ingredients brought on by the global pandemic, according to...
The US Food and Drug Administration has sent another warning letter in its decade-long campaign against the use of the weight loss drug sibutramine in dietary supplements.
By By Steve Mister, President & CEO, Council for Responsible Nutrition
We all want an expedient solution to the stalemate with FDA over the legal status of cannabidiol (CBD), but the call to allow FDA to set a maximum safe level for CBD is antithetical to the law governing dietary supplements, DSHEA.
Nestlé makes available a report outlining efforts to comply with formula marketing guidelines that in recent years has been a subject of contention for the owners of the Gerber and NAN baby food brands.
Today (Aug 24) marks a deadline for public comment on a FDA request for input on the abuse potential of a number of drug substances, including kratom. Even as the regulatory winds shift around the ingredient, analytical labs are lining up to service...
3D printing technology can be applied to pretty much any industry. It's prevalent in aerospace, jewelry and prosthetics. Even dietary supplements can be made this way.
The Natural Products Association has filed a citizen’s petition asking FDA to acknowledge NAC as a legal dietary ingredient. The molecule, which has been on the market for decades, was ruled last year as violative by the Agency.
The maker of a beverage claiming to treat anxiety disorders has received a warning letter form the US Food and Drug Administration for both alleged drug claims and the inclusion of an illegal dietary ingredient.
The US Food and Drug Administration has rejected two New Dietary Ingredient Notifications for CBD ingredients. Industry stakeholders said the fact of the rejections and some of wording used in the letters makes it clear that new legislation is likely...
Food Supplements Europe (FSE) has made available a series of recommendations aimed at growers and botanical collectors to reduce the presence of Pyrrolizidine Alkaloids (PA) in food supplements.
