AHPA
AHPA Submits Vinpocetine Comments to FDA
The American Herbal Products Association (AHPA) recommends the Secretary of Health and Human Services (HHS) consider initiating rulemaking to declare vinpocetine to be lawful dietary ingredient in comments submitted to the U.S. Food and Drug Administration (FDA). AHPA also strongly encouraged FDA to clarify that if vinpocetine is either found to be currently in the ...
AHPA Issues Slack-fill Guidance
The American Herbal Products Association (AHPA) has published slack-fill guidance to help the regulated supplement industry inform consumers and comply with all relevant federal requirements. The difference between the capacity of a container and the volume of product inside is known as “slack-fill.” The U.S. Food and Drug Administration (FDA) regulates how food (including dietary ...
FDA Releases Revised Draft of NDI Guidance; AHPA Convenes Working Group for Comments
The Food and Drug Administration (FDA) today released revised draft guidance for new dietary ingredients (NDIs) to be published in the Federal Register on Friday, Aug. 12. The revised draft replaces FDA’s 2011 draft. The guidance, “Draft Guidance for Industry: Dietary Supplements: New Dietary Ingredient Notifications and Related Issues,” is subject to a 60-day comment period. ...
Wilson Lau to Chair AHPA Board of Trustees
The American Herbal Products Association (AHPA) Executive Committee has appointed Wilson Lau as chair of the AHPA Board of Trustees until March 2017. Lau is the vice president of sales at nuherbs Company and has served on the AHPA board since 2008. He is also chair of AHPA’s Tea and Infusion Products Committee. “AHPA appreciates ...
Industry Urges FDA to Define “Natural”
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 ...
Senator Blumenthal Withdraws Amendment to Limit Military Access to Supplements
Senator Richard Blumenthal (D-CT) withdrew his amendment to the FY 2017 National Defense Authorization Act (NDAA) that would require supplements sold on military bases to be verified by a third-party amid strong opposition by the supplement industry. Enacted on an annual basis by Congress, NDAA legislation establishes budget and policy parameters for the Department of ...
AHPA Appoints Robert Wildman to Chair Sports Nutrition Committee
The American Herbal Products Association (AHPA) appointed Dr. Robert Wildman, chief science officer at Post Active Nutrition Brands, as the new chair of the Sports Nutrition Committee during a meeting at Natural Products Expo West in Anaheim, CA. Wildman succeeds Ray Jaglowski, vice president of technical and regulatory at Twinlab Corp., who chaired the committee ...
AHPA Advocacy Spurs Correction of FDA’s Dietary Supplement Labeling Guide
The U.S. Food and Drug Administration (FDA) has corrected its Dietary Supplement Labeling Guide after the American Herbal Products Association (AHPA) notified the agency of inaccurate information posted online. AHPA notified FDA in September 2015 that its guidance for industry titled “A Dietary Supplement Labeling Guide,” included one detail that contradicted current law and FDA regulations. ...
AHPA and UNPA Launch Campaign to Educate State AGs
The American Herbal Products Association (AHPA) and the United Natural Products Alliance (UNPA) have launched a joint campaign to develop working relationships with state attorneys general (AG) and educate them about the herbal supplement industry. This is the latest effort by AHPA and UNPA to ensure state AGs have an accurate understanding of the industry. ...
Frontline Segment: Skewed & Misleading, AHPA Says
A segment aired on January 19 on PBS’ Frontline presented dietary supplements as inherently unsafe by misrepresenting the rigorous safety provisions established for these products under the Federal Food, Drug and Cosmetics Act, the strict liability statute under which supplements are regulated. The segment, titled “Supplements and Safety,” relied on anecdotal reports of noncompliant products ...
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