U.S. Food and Drug Administration
FDA Announces New Attention to Dietary Supplement Regulations
FDA (U.S. Food and Drug Administration) Commissioner Scott Gottlieb, MD, has announced that the agency is planning “new efforts to strengthen regulation of dietary supplements by modernizing and reforming FDA’s oversight,” with a goal of implementing “one of the most significant modernizations of dietary supplement regulation and oversight in more than 25 years.” The commissioner’s ...
NPA Asks for Consistent National Standard for Plant-based Food Labeling
The Natural Products Association (NPA) recently urged the U.S. Food and Drug Administration (FDA) to adopt a policy of enforcement discretion on standards of identity for products that use dairy names to describe plant-based products such as “soy milk” and “almond milk.” “Plant-based products, as long as they are properly qualified, like almond milk, soy ...
AHPA Issues Updated Slack-fill Guidance
The American Herbal Products Association (AHPA) has updated its Slack-Fill Guidance to help the regulated supplement industry inform consumers and comply with all relevant federal requirements. This guidance was originally published in November 2016 and has been reorganized and edited for clarity, with one substantive revision in the discussion on “Label statements and fill lines” ...
Nutritional Supplements Access Preserved in Arizona
A proposal that would have drastically limited access to safe, legal and popular products for Arizonans was changed recently with the help of the Natural Products Association (NPA) and the American Herbal Products Association (AHPA), who worked with the Arizona Board of Pharmacy and other state policymakers on the issue. The proposal under consideration would have ...
New Farm Bill is Imminent as it Passes House and Senate
On the evening of Dec. 10, the 2018 Farm Bill House/Senate Conference Committee released its Conference Report. The 807-page document is nearly half a foot tall. Hemp is discussed in only a few handfuls of pages. As of press time, the Senate passed the bill on Dec. 11 by a vote of 87 to 13; ...
FDA Announces New Final Guidances on Revised Nutrition Labeling
On November 2, the U.S. Food and Drug Administration (FDA) announced two new final guidances to help companies revise nutrition labels for conventional foods and dietary supplements to comply with the new regulations. One document deals with the definition of a single-serving container, reference amounts customarily consumed, which are used by companies to determine serving ...
Trade Associations Warn Consumers of Dangerous Substance Illegally Marketed as a Dietary Supplement
The dietary supplement industry sounded the alarm about the dangers of “phenibut,” a substance being illegally marketed in products fraudulently labeled as dietary supplements. Developed and used as a drug in the former Soviet Union for its supposed brain-enhancing properties, phenibut is not approved as a drug in the United States, nor does it meet ...
Efficient Regulatory Structure Critical to Protecting Consumers and Public Health, says NPA
The Natural Products Association (NPA) has called for a streamlined and efficient regulatory structure to protect consumers and public health as the U.S. Food and Drug Administration (FDA) implements its “Comprehensive, Multi-Year Nutrition Innovation Strategy.” “NPA supports the goals of FDA in its plans for the Multi-Year Nutrition Innovation Strategy and its efforts to promote ...
FDA Asks for Consumer Input on Labeling Plant-Based Products, NPA Responds
The U.S. Food and Drug Administration (FDA) has issued a request for information as it examines its approach to the use of dairy food names like “milk,” “cheese,” or “yogurt” in the labeling of plant-based foods and beverages. Earlier this year, FDA Commissioner Scott Gottlieb announced FDA’s Nutrition Innovation Strategy (NIS) in a speech to the National ...
New Draft Guidance for Probiotic Labeling Could Yield Inaccurate Product Labels, CRN Says
The U.S. Food and Drug Administration (FDA) recently released a draft guidance entitled “Policy Regarding Quantitative Labeling of Dietary Supplements Containing Live Microbials” to advise firms that manufacture, market or distribute dietary supplements that contain live microbial ingredients of the conditions under which the FDA intends to exercise enforcement discretion to allow firms to declare ...
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