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HHS, FDA Phasing Out Petroleum-based Synthetic Food Dyes, Industry Responds

by Shari Barbanel | May 1, 2025

On April 22, the U.S. Food and Drug Administration (FDA) and Department of Health and Human Services (HHS) announced a plan to phase out all petroleum-based synthetic dyes from the nation’s food supply as part of the Make America Healthy Again (MAHA) movement. FDA is taking numerous actions including establishing a national standard and timeline ...

JAMA Research Letter Raises False Alarm Over Levels of Melatonin in Gummies, CRN Says

by Shari Barbanel | April 28, 2023

The Council for Responsible Nutrition (CRN) has responded to a newly published research letter (“Quantity of Melatonin and CBD in Melatonin Gummies Sold in the U.S.”) appearing in the Journal of the American Medical Association (JAMA), which suggests that clinicians should “advise” parents that the levels of melatonin in gummies are “unpredictable.” Melatonin is often ...

NPA Files Citizen Petition with FDA

by Shari Barbanel | August 23, 2021

In a Citizen’s Petition to the U.S. Food and Drug Administration (NPA), the Natural Products Association (NPA) requested that N-acetyl-L-cysteine (“NAC”) not be excluded from the definition of a dietary supplement. “The Food and Drug Administration has not established a public health risk for NAC,” said Daniel Fabricant, PhD, president and CEO of NPA. “Not ...

FDA’s Request for Supplement Registration Doesn’t Unburden Industry, Says NPA

by Shari Barbanel | March 25, 2019

The Natural Products Association (NPA) recently asked Congress to reject the U.S. Food and Drug Administration’s (FDA) budget request for a product registration system for nutritional supplements, as it’s unclear of what value is added to the agency’s mission of promoting and protecting public health.      “The administration has been clear that they want to unburden ...

FDA, Stakeholders Meet, Mull Over Pre-DSHEA Dietary Ingredients List

by Shari Barbanel | October 10, 2017

On October 3, the U.S. Food and Drug Administration (FDA) held a public meeting to discuss the development of a list of pre-Dietary Supplement Health and Education Act of 1994 (DSHEA) dietary ingredients. According to a release from Washington, D.C.-based law firm Keller and Heckman LLP, the meeting featured two stakeholder panels that presented on ...

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