dietary supplements
NOW Presses Amazon to Act Against Deceptive Dietary Supplement Sellers
NOW continues to press Amazon to act against sellers of dietary supplements seeking to trick consumers into thinking their products are quality, the company stated. In the latest tactic, NOW said it spotted a brand posting certificates of analysis from a third-party testing lab on their website confirming fill weight. Not identity, potency or purity–just ...
Lawsuits Filed Against Olly, P&G, Alleging Deceptive Advertising of Melatonin Supplements
On Friday, June 24, Dovel & Luner, a litigation boutique law firm, filed a federal class action lawsuit against Olly Public Benefit Corporation and The Proctor & Gamble Company on behalf of consumers nationwide who purchased melatonin supplements. The lawsuit alleges that Olly and Proctor & Gamble misled consumers by inaccurately dosing and labeling its ...
Rhode Island Senate Passes Amended Legislation Restricting Dietary Supplement Accessibility
On June 7, the Rhode Island State Senate approved an amended version of S. 2613, which prohibits the sale of certain dietary supplements to youths under the age of 18. The original version would have prohibited dietary supplements from being directly accessible to customers and mandate that only retail clerks may have access to them; ...
Video: Interview with Steve Mister, Council for Responsible Nutrition
Steve Mister, President & CEO, Council for Responsible Nutrition (CRN) met with Vitamin Retailer to discuss the organization’s latest news, the pandemic’s impact on the natural products industry and more. For more information, visit www.crnusa.org.
Senate HELP Committee Leaders Looks to Advance FDASLA With Controversial Provisions
On June 13, the United States Senate ignored the dietary supplement industry by continuing to move forward with provisions left in the Food and Drug Administration Safety and Landmark Advancement Act (FDASLA), according to the Natural Products Association (NPA). The NPA requested from the Senate HELP committee in a series of letters that the committee strike the ...
Video: Interview with Karen Howard, Organic & Natural and Brian Terry, Nordic Naturals
Karen Howard, CEO & Executive Director, Organic & Natural Health Association and Brian Terry, Director of Sales, Nordic Naturals, met with Vitamin Retailer to discuss their partnership with the Williams-Franklin Foundation, involvement with the HBCU scholarship fund and more. For more information, visit www.organicandnatural.org and www.nordic.com.
CRN and CHPA Comment on Report of Increased, Unintentional Pediatric Melatonin Ingestion
The Council for Responsible Nutrition (CRN) and the Consumer Healthcare Products Association (CHPA) have provided their comments on the recent report of increased, unintentional pediatric melatonin ingestion. A 10-year study, released by the Centers for Disease Control and Prevention (CDC) on Thursday, June 3, found a sharp increase in the use of melatonin by children ...
Rhode Island Senate Considers Legislation Restricting Dietary Supplement Accessibility
The Rhode Island State Senate is advancing through the chamber S. 2613, which prohibits dietary supplements from being directly accessible to customers and mandates that only retail clerks may have access. While the bill does not regulate internet sales of dietary supplements in Rhode Island, it requires brick and mortar retailers to post a warning ...
CRN Objects to Missing Protections in FDA Safety and Landmark Advancements Act
On May 27, the Council for Responsible Nutrition (CRN) issued a statement by Steve Mister, president and CEO, regarding the FDA Safety and Landmark Advancements Act (FDASLA) introduced by the Senate HELP Committee. “The Council for Responsible Nutrition is disappointed with the FDA Safety and Landmark Advancements Act introduced today. “CRN has led the dietary supplement industry ...
NPA Responds as Durbin-Braun Proposal for Dietary Supplements Makes Its Way into PDUFA
On May 17, the United States Senate Health, Education, Labor, and Pensions Committee (HELP) released a discussion draft of its legislation to reauthorize FDA user fees for drugs, biologics and medical devices package, which includes the controversial and divisive Durbin-Braun premarket approval concept and more that would be damaging to the industry, according to the ...
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