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2019 Industry Forecast
The Participants Are: • Jonathan Emord, Esq., President, Emord & Associates, Washington, D.C., www.emord.com • Daniel Fabricant, PhD, President and CEO Natural Products Association (NPA), Washington, D.C., www.npanational.org • Kurt Jetta, PhD, Executive Chairman and Founder, TABS Analytics, Shelton, CT, www.tabsanalytics.com • Mark LeDoux, Chair and CEO, Natural Alternatives International (NAI), Carlsbad, CA, www.nai-online.com • ...
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; ...
What is Slack-fill & Why You Need to Know
It seems that we spend so much time thinking about the product that goes inside the bottle or box, that we sometimes give very little thought to the package itself. There are several issues concerning product packaging that deserve your attention, including the question of whether the container itself is potentially “misleading.” The possibility of ...
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 ...
AHPA NDI Database Shows Increase of Recent Notifications Filed Successfully
Eight of the 21 new dietary ingredient (NDI) notifications released by the U.S. Food and Drug Administration (FDA) between January 1, 2018 and May 31, 2018 were filed by the agency without substantive comment. The vast majority of these (17) complied with all submission regulations (21 CFR 190.6). The recently received data have been analyzed and ...
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