
From maximum vitamin and mineral levels to the future of EFSA, speakers at the recent “Brexit Impact” webinar hosted by AHPA and CRN explain what companies should watch out for.

From maximum vitamin and mineral levels to the future of EFSA, speakers at the recent “Brexit Impact” webinar hosted by AHPA and CRN explain what companies should watch out for.

AHA recommends children aged 2–18 consume no more than six teaspoons of added sugars per day and limit consumption of sugary drinks to less than 8 ounces per week.

“To battle pointlessly only gives the industry’s critics further ammunition that we oppose any effort to rein in the bad actors that lurk around the fringes of the industry,” says CRN’s Steve Mister.

Plus: Will FDA now step up its game of NDI enforcement?

Industry should remain on high alert over whether FDA's "chemical alteration" language in its revised new dietary ingredient draft guidance will require a broad swath of industry companies to submit NDI notifications, expert says.

The second generation of USP’s Food Fraud Database includes added capabilities that make it easier for users to identify historical trends and vulnerabilities for food fraud.

The warnings span everything from products for hangover relief to picamilon-containing dietary supplements.

Just one day after FDA finally issued its revised new dietary ingredient (NDI) draft guidance for dietary supplements, the agency today released its Generally Recognized as Safe (GRAS) final rule for food ingredients.

FDA today released its long-awaited revised new dietary ingredient (NDI) draft guidance with two major changes the dietary supplement industry will likely hail as good news.

The USDA now has two years to hammer out details for implementing the federal GMO-disclosure law.

The Natural Products Association has launched a new database of more than 400 dietary supplement warning letters from FDA, as well as other regulatory enforcement actions taken since 2008.

From cat scans to particle structure, ingredient suppliers are using advanced methods to help food formulators cut sodium.

Fiber suppliers at this year’s Institute of Food Technologists Annual Meeting & Food Expo told Nutritional Outlook that while they are confident FDA will eventually consider their ingredients to be dietary fibers, the path to FDA approval is unclear.

Rimfrost’s Sublime PL60 krill oil, which debuted last fall, features a phospholipid content of up to 60% and high levels of choline, astaxanthin, and omega-3 DHA and EPA.

The FTC accused Herbalife of misleading consumers by suggesting those consumers could earn significant income by selling Herbalife products when in fact most did not.

President Obama is expected to sign the legislation, which would nullify Vermont’s mandatory GMO-labeling law.

The controversial bill, which would allow food companies to direct consumers online for GMO disclosures, passed in the Senate last night by a 63–30 margin.

Companies who choose to invest in in-house manufacturing may see unique dividends, says one equipment supplier.

The Council for Responsible Nutrition’s annual events will take place from October 26–29 at the Ritz-Carlton, Laguna Niguel (Dana Point, CA).

Underwriters Laboratories and the Council for Responsible Nutrition expect to launch the new online registry by the end of 2016, with beta testing planned for the coming months.

The bill would have required supplement manufacturers and retailers operating in Puerto Rico pay higher fees and submit additional product information.

Market researcher Euromonitor International took a look at how “Brexit” could negatively affect the consumer packaged foods industry.

If the bill were to pass, companies could disclose GMO ingredients through on-package text, symbols, or digital codes that direct consumers to more information online.

Algae Life Sciences recently announced it had 239 “FDA-allowed” structure-function claims for its AstaZine astaxanthin ingredient. But its competitor, AstaReal, challenges the significance of these claims.

More than 60 supplement industry executives sat down with members of the U.S. Congress last week to discuss pressing issues facing the industry.

FDA’s new draft guidance seeks to reduce daily sodium intake to 2300 mg per person over the course of 10 years.

FDA says KIND can continue to use the term “healthy” on its packaging because it is an expression of “corporate philosophy” and not a health claim. Will other companies follow suit?

The new health claim applies to foods containing at least 0.5 grams of EPA and DHA combined.

The company is now certified to UL’s National Brand Certification Program (NBCP).

Manufacturers have up to two years to comply with the new label for food and beverage packaging.