Federal Food
NPA Argues New York Supplements Ban Is Unconstitutional
On Dec. 5, the Natural Productions Association (NPA) filed a complaint in the U.S. District Court for the Eastern District of New York, asserting the recent supplements ban in New York is unconstitutional. The law bans the sale of supplements to anyone under 18 years of age and in certain situations may require a prescription to ...
FDA Warns Selling of Topical CBD Products Violates FD&C Act
On March 22, the U.S. Food and Drug Administration (FDA) stated that it has issued warning letters to two companies for selling topical pain relief products labeled as containing cannabidiol (CBD) in ways that violate the Federal Food, Drug and Cosmetic Act (FD&C Act). Specifically, the warning letters addressed the illegal marketing of unapproved drugs ...
FDA Issues CBD Warning Letters
The U.S. Food and Drug Administration (FDA) recently issued warning letters to 15 companies for, according the agency, illegally selling products containing cannabidiol (CBD) in ways that violate the Federal Food, Drug, and Cosmetic Act (FD&C Act). The FDA also published a revised Consumer Update detailing safety concerns about CBD products more broadly. The agency stated, based ...
New Book Compiles First Ever List of Pre-DSHEA Dietary Ingredients
A new book from the Natural Products Association (NPA) compiles the first ever list of pre-DSHEA (Dietary Supplement Health and Education Act of 1994) dietary ingredients. The NPA book, titled Pre-DSHEA List of Old Dietary Ingredients, is available for pre-sale starting until the end of the year for members, non-members, federal agencies and non-governmental organizations (NGOs). ...
Associations Submit Comments on Revised NDI Draft Guidance
Some of the natural product industries’ leading associations, including the American Herbal Products Association (AHPA), Council for Responsible Nutrition (CRN), American Botanical Council (ABC) and Natural Products Association (NPA), recently submitted comments to U.S. Food and Drug Administration (FDA) in response to the agency’s revised New Dietary Ingredient (NDI) Draft Guidance. FDA issued on August ...
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 ...
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