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NPA Works to Repeal Puerto Rico Order on Supplements

by Corinne Anderson | May 23, 2016

The Natural Products Association (NPA) is meeting with members of the House of Representatives to overturn an administrative order (Administrative Order #346) issued by the Commonwealth of Puerto Rico’s Department of Health that would raise prices for dietary supplement and natural products consumers and adds requirements for retailers/distributors inconsistent with federal law.  The NPA is […]

Industry Urges FDA to Define “Natural”

by Corinne Anderson | May 16, 2016

The American Herbal Products Association (AHPA) submitted comments to the 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% natural” and “made with natural [named ingredient(s)]”) for the labeling of human food products, and other products regulated by […]

FDA Reverse Stance: Affirms KIND Can Use “Healthy” on Labels

by Corinne Anderson | May 10, 2016

 KIND Healthy Snacks (KIND)  announced it has been notified by the U.S. Food & Drug Administration (FDA) that it can use the term healthy on its packaging as it had before – a reversal of the position the FDA took more than a year ago. The acknowledgment comes after much public conversation among health and nutrition leaders about […]

Unapproved Ephedrine-like Stimulant Found in Dietary Supplements

by Corinne Anderson | May 9, 2016

Researchers from global public health organization NSF International, Harvard Medical School, the National Center for Natural Products Research (NCNPR) at the University of Mississippi and the National Institute for Public Health and the Environment in the Netherlands (RIVM) have found the unapproved pharmaceutical stimulant oxilofrine in 14 over-the-counter dietary supplement products. Their research on oxilofrine […]

FDA Approves Folic Acid to be Added to Masa Flour

by Corinne Anderson | April 19, 2016

The U.S. Food and Drug Administration (FDA) has decided to allow manufacturers to fortify their corn masa foods with folic acid. “Folic acid is a synthetic form of folate, a B vitamin that helps prevent severe defects of the brain and spinal cord when consumed by women before and early [on] in pregnancy,” an NPR […]

NPA Submits Comments on Voluntary GE Labeling

by Corinne Anderson | December 30, 2015

The Natural Products Association (NPA) submitted comments regarding the US Food and Drug Administration’s (FDA) Draft Guidance for Industry on Voluntary Labeling Indicating Whether Foods Have or Have Not Been Derived From Genetically Engineered (GE) Plants. The FDA’s position on the labeling of genetically engineered foods is unchanged from its initial 1992 policy statement. While NPA […]

Supplements are Elevated to “Office” Status Within FDA

by Corinne Anderson | December 22, 2015

The five trade associations representing the dietary supplement industry welcomed the elevation of the Division of Dietary Supplement Programs (DDSP) to an “Office” status within the Food and Drug Administration’s (FDA) Center for Food Safety and Applied Nutrition (CFSAN) on December 21, 2015. The groups—the American Herbal Products Association (AHPA), the Consumer Healthcare Products Association […]

CRN Supports FDA Against Consumer Access to Powdered Caffeine

by Corinne Anderson | December 15, 2015

The U.S. Food and Drug Administration (FDA) issued warning letters to five distributors of pure powdered caffeine because the products are dangerous and present “significant or unreasonable risk of illness or injury to consumers,” the FDA said. The Council for Responsible Nutrition (CRN) released a statement supporting the FDA and its decision. “We have been, […]

FDA Determines GE Salmon Safe

by Corinne Anderson | November 20, 2015

“After an exhaustive and rigorous scientific review, FDA [Food and Drug Administration] has arrived at the decision that AquAdvantage salmon is as safe to eat as any non-genetically engineered (GE) Atlantic salmon, and also as nutritious,” the FDA report stated. The FDA scientists evaluated data submitted by the manufacturer, AquaBounty Technologies, and other peer-reviewed data, […]

NPA Welcomes FDA Process to Define “Natural”

by Corinne Anderson | November 18, 2015

The Natural Products Association (NPA) responded to recent steps taken by the U.S. Food and Drug Administration (FDA) to define the term “natural” on food labels. “It’s about time that natural be defined by experts and no Madison Avenue ad executives,” said Dan Fabricant, PhD, executive director and CEO of the NPA. “NPA strongly supports […]

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