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Daniel Fabricant


New National Survey Shows Strong Public Support for Natural Health Options

by Angela Sabarese | October 17, 2022

A new national poll from a coalition of organizations with an interest in natural health, conducted by the Marist Poll, shows that 70 percent of Americans are more likely to support a congressional candidate who will protect the public’s access to dietary supplements and other natural and homeopathic remedies. The Marist Poll, one of the ...

NPA Urges California to Weigh Enforcement of Legislation Restricting Access to Dietary Supplements

by Angela Sabarese | September 13, 2022

On Sept. 8, following the passage of California’s AB 1341, which restricts access to dietary supplements and, in certain situations, requires a prescription to access these health products, the Natural Products Association (NPA) sent a letter to the California Department of Public Health Director Tomas J. Aragón urging the director to recognize the importance of ...

FDA’s Long-Sought Guidance on NAC Follows NPA’s Lawsuit and Citizen’s Petition

by Angela Sabarese | August 2, 2022

Following a Citizen’s petition and lawsuit filed by the Natural Products Association (NPA) against the U.S. Food and Drug Administration (FDA) for a dietary supplement issued enforcement discretion for N-Acetyl-Cysteine (NAC) has resulted in the agency issuing final guidance. “This is a big win but it is bittersweet for sure. Although it was NPA’s leadership ...

NPA Applauds New Jersey Proposal to Recognize July 9 as Creatine Day

by Angela Sabarese | July 22, 2022

The Natural Products Association (NPA) has applauded New Jersey State Senator Bob Singer (30-Lakewood) for introducing a Senate Joint Resolution recognizing July 9 as Creatine Day in New Jersey. “Creatine is one of the most popular nutritional supplements because of its long history of strength and muscle health,” said Daniel Fabricant, Ph.D., president and CEO ...

Senator Burr Takes Strong Position Against Including Dietary Supplement Provisions in FDA User Fee Bill Package

by Angela Sabarese | July 19, 2022

On July 14, Senator Richard Burr (R-NC), the ranking member of the Senate HELP Committee and a central negotiator in the conference proceedings, introduced a clean reauthorization of FDA User Fee Programs which does not include controversial dietary supplement provisions. Senator Burr cited concerns over the Senate’s ability to pass the Food and Drug Administration ...

NPA, CRN Release Statements on Preventive Services Task Force Guidance on Dietary Supplements

by Angela Sabarese | June 23, 2022

The Natural Products Association (NPA) and the Council for Responsible Nutrition (CRN) have issued statements in response to recent findings by the U.S. Preventive Services Task Force (USPSTF). NPA commented on what USPSTF found in relation between the use of beta carotene and vitamin E for the prevention of cardiovascular disease and cancer. Ultimately, “The ...

Rhode Island Senate Considers Legislation Restricting Dietary Supplement Accessibility

by Angela Sabarese | June 1, 2022

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 ...

NPA Responds as Durbin-Braun Proposal for Dietary Supplements Makes Its Way into PDUFA

by Angela Sabarese | May 23, 2022

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 ...

NPA Applauds House Energy & Commerce Committee for Excluding Dietary Supplements from User-fee Reauthorization Legislative Package

by Angela Sabarese | May 9, 2022

On May 4, the United States House of Representatives Energy and Commerce Committee unveiled its FDA User Fee legislative package, which did not include the “mandatory product listing” concept in its legislation to reauthorize FDA user fees for drugs, biologics and medical devices. “The NPA applauds Chairman Frank Pallone and Republican Leader Cathy McMorris Rodgers ...

Durbin, Braun Introduce Legislation to Mandate Product Listings for Dietary Supplements

by Angela Sabarese | May 3, 2022

U.S. Senate Majority Whip Dick Durbin (D-IL) and U.S. Senator Mike Braun (R-IN) introduced the Dietary Supplement Listing Act of 2022, bipartisan legislation to require dietary supplement manufacturers to list their products with the Food and Drug Administration (FDA). The Dietary Supplement Listing Act of 2022 would require companies to provide FDA with vital information about their products, ...

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