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FDA Fails to Deliver Congressionally Mandated Report on CBD Regulations

by Shari Barbanel | February 26, 2020

The U.S. Food and Drug Administration (FDA) failed to meet its deadline to provide a Congressionally mandated report on how it plans to regulate CBD. Congress instructed the FDA in last year’s spending bill to adopt an enforcement discretion policy within 120 days and provide an update of its progress after 60 days. The agency’s first report ...

NPA Urges Health Care Professionals to Report Adverse Events for Dietary Supplements

by Shari Barbanel | January 16, 2020

In a letter to leading medical societies, the Natural Products Association (NPA) is urging that health care professionals make recommendations for reporting adverse events for dietary supplements. Manufacturers of dietary supplements are required to submit all information pertaining to adverse events associated with their products to the FDA (U.S. Food and Drug Administration). “Adverse events ...

Senate Confirms Hahn as FDA Commissioner

by Shari Barbanel | December 16, 2019

In a 72-18 Senate vote, Stephen Hahn, MD, FASTRO was confirmed as the new head of the U.S. Food and Drug Administration (FDA), taking charge at a regulatory agency that oversees products ranging from complex cancer drugs, to food, cosmetics, tobacco and CBD. “We look forward to working with Dr. Hahn and his staff to ...

President Trump Nominates Stephen Hahn as FDA Commissioner

by Shari Barbanel | November 6, 2019

According to Politico, President Donald Trump announced last week that he will nominate Stephen Hahn, MD, FASTRO, a cancer specialist and hospital administrator, to lead the FDA (U.S. Food and Drug Administration). Trump had been rumored to make this selection for several months. If confirmed by the Senate, the top FDA post would mark Hahn’s first ...

House of Representatives Instructs FDA to Regulate CBD

by Shari Barbanel | July 16, 2019

Legislation passed the House of Representatives on June 25 that would appropriate $100,000 for the U.S. Food and Drug Administration (FDA) to perform a Health Hazard Evaluation (HHE) and set a safe level of CBD for consumers to use each day. The process would follow the same precedent as red yeast rice, which allows a natural product to ...

NPA Responds to Findings of New Study on Cancer Risk Among Smokers Taking Vitamin B Supplements

by Shari Barbanel | August 25, 2017

The Natural Products Association (NPA) has rejected a study by researchers blaming vitamin B use by male smokers for an increased risk of cancer.  Dan Fabricant, PhD, president and CEO of NPA pointed to environmental factors and tobacco use as the more likely cause for increased cancer risk. Dr. Fabricant is a former head of ...

Industry Urges FDA to Define “Natural”

by Shari Barbanel | May 18, 2016

The American Herbal Products Association (AHPA) submitted comments to the U.S. Food and Drug Administration (FDA) encouraging the agency to establish, through rulemaking, a regulatory definition for the term “natural” (and possibly other terms, such as “100 percent natural” and “made with natural [named ingredient(s)]”) for the labeling of human food products, and other products ...

NPA Calls for Changes at FDA to Give Consumers Access to More Natural Sunscreen Products

by Shari Barbanel | February 8, 2016

The Natural Products Association (NPA) in two recent public filings with the U.S. Food and Drug Administration (FDA) encouraged the adoption of standards that would result in the availability of more natural ingredients in sunscreen for consumers.  NPA called on the FDA to clarify what it considers an active ingredient in sun protection products and ...

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