Daniel Fabricant
NPA Issues Statement in Response to FDA’s Refusal to Hold Public Hearing Regarding NMN
On July 20, the U.S. Food and Drug Administration (FDA) rejected a request by Rep. Jeff Duncan (R-SC), a member of the House Energy and Commerce Committee, to hold a public hearing on the agency’s position on nicotinamide mononucleotide (NMN). FDA stated that a public comment period would be sufficient. In response, the Natural Products ...
WHO Releases Results of Hazard and Risk Assessment on Aspartame, Associations Comment
On July 14, the World Health Organization (WHO) International Agency for Research on Cancer (IARC) and the WHO Food and Agriculture Organization (FAO) Joint Expert Committee on Food Additives (JECFA) released results about the health impact of aspartame. The two groups within the organization have come to different conclusions, with IARC stating that aspartame is ...
Trade Associations Respond to FDA’s Denial of CBD Citizen Petitions
The Natural Products Association (NPA), the Council for Responsible Nutrition (CRN) and the Consumer Healthcare Products Association (CHPA) have responded to the U.S. Food and Drug Administration’s (FDA) denial of the associations’ CBD Citizen Petitions on Jan. 26. “This is an astonishing dereliction of duty, especially compared to the agility and professionalism the agency showed ...
MPL for Dietary Supplements Omitted From Omnibus Spending Bill
The Omnibus Spending Bill was released on December 20 without including the controversial Mandatory Product Listing (MPL) of dietary supplements. Daniel Fabricant, PhD, president and CEO of the Natural Products Association (NPA), stated, “This is a big win for consumers, for innovation, and for access to the healthy products that millions of Americans rely on ...
CRN Refutes NPA’s Comments on its Support of Dietary Supplement Listing Act
The Council for Responsible Nutrition (CRN) released a statement saying that it has responded to “false information being propagated on social media and other platforms by the Natural Products Association (NPA) regarding effects of the bi-partisan Dietary Supplement Listing Act, as well as the nature of CRN’s support for the proposal and Sen. Richard Durbin’s ...
Following Final NAC Guidance and Marketplace Stabilization, NPA Withdraws FDA Lawsuit
After securing final guidance for N-Acetyl-Cysteine (NAC) through a citizen petition and lawsuit, the Natural Products Association (NPA) dismissed its case against the U.S. Food and Drug Administration (FDA), which preserves legal rights and standing should additional action be necessary. The guidance also initiates the process for export certificates for NAC, which was a primary ...
CA Governor Gavin Newsom Vetoes Age-restrictive Legislation for Weight-loss Supplements
California Gov. Gavin Newsom has vetoed AB 1341, which would have restricted the sale of weight loss supplements to individuals under the age of 18. The legislation, which was introduced by Assembly member Cristina Garcia and staff last year, would have prohibited retailers from selling the dietary supplements to those without a valid prescription or ...
NPA: California Bill Restricting Supplement Access Should Be Vetoed
The Natural Products Association (NPA) has called the passage of a California bill to restrict access to dietary supplements a slap in the face to public health and consumer choice. The California bill, AB 1341, restricts access to dietary supplements and in certain situations requires a prescription to access these health products. While the bill does ...
FDA’s Long-sought Guidance on NAC Follows NPA’s Lawsuit and Citizen’s Petition
Following a Citizen’s petition and lawsuit filed by the Natural Products Association (NPA) against the U.S. Food and Drug Administration (FDA) for a dietary supplement issued enforcement discretion for N-Acetyl-Cysteine (NAC) has resulted in the agency issuing final guidance. “This is a big win but it is bittersweet for sure. Although it was NPA’s leadership ...
NPA, CRN Respond to Research Showing Supplements With Banned Ingredients are Still on the Market
A study recently published in JAMA by Pieter A. Cohen, MD; Bharathi Avula, PhD; and Kumar Katragunta, PhD, et al, has found that supplements with banned ingredients are still on the market despite the companies having received warning letters from the U.S. Food and Drug Administration (FDA). The study stated that “Some dietary supplements are adulterated ...
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