DSHEA Daily Digest – 2026-08-25 – Vol 5 Iss 5
DSHEA Daily Digest Daily Digest August 25, 2026 Volume 5, Issue 5 What’s Inside Today BBB National Programs’ National Advertising Division decided a challenge Kenvue
August 25, 2026
Our Media & Newsroom serves as a vital resource, offering insights and updates that keep our community informed. Explore key developments, important announcements, and resources that elevate our mission.
Welcome to the official media hub of the DSHEA Preservation Alliance. Here, journalists, researchers, and stakeholders can access reliable information, timely updates, and expert perspectives on the policies, challenges, and successes shaping the future of dietary supplement regulation. Whether you’re covering legal developments, tracking FDA activity, or exploring DSHEA’s impact on public health and innovation, our newsroom offers curated resources to support your work. Browse our press releases, statements, and recent headlines—or reach out directly for customized support. We’re here to ensure clarity, credibility, and context in every story.
DSHEA Daily Digest Daily Digest August 25, 2026 Volume 5, Issue 5 What’s Inside Today BBB National Programs’ National Advertising Division decided a challenge Kenvue
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DSHEA Weekly Digest – August 11, 2026 Weekly Digest August 11, 2026 Volume 5, Issue 2 What’s Inside This Week The self-affirmed GRAS era may
DSHEA Weekly Digest – August 4, 2026 Weekly Digest August 4, 2026 Volume 5, Issue 1 What’s Inside This Week Federal cannabinoid policy took center
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News
By Matt SandgrenMatt is the executive director of the Orrin G. Hatch Foundation. A 15-year veteran of Capitol Hill, he served as senior counsel on the Senate Judiciary Committee and as Senator Hatch’s chief of staff. If, like millions of other Americans, you take a multivitamin, herbal supplement or omega-3 fatty acid...
News
The Wall Street Journal reported on the booming longevity industry and the regulatory challenges faced by companies marketing NMN supplements. The article highlights the dispute between supplement companies and pharmaceutical firms over NMN’s classification and the FDA’s stance on its legality as a dietary supplement.
...Newsletter
A federal court mandated the FDA to halt enforcement actions against NMN vendors and required the agency to address the NPA’s pending citizen petition. This decision provides temporary relief to NMN supplement manufacturers and consumers.
...Press Release
The NPA hailed the court’s decision to stay the NMN lawsuit as a “monumental victory,” emphasizing that the FDA exceeded its authority and must adhere to the law’s provisions. The ruling allows NMN supplements to remain on the market while the FDA reviews the citizen petition.
...News
A federal court granted a joint motion filed by the NPA and FDA to stay proceedings in the NMN lawsuit, pending the FDA’s response to the NPA’s citizen petition. The FDA indicated it would respond to the petition by July 31, 2025, and would not prioritize enforcement actions against NMN...
Newsletter
The Natural Products Association (NPA) filed a lawsuit challenging the FDA’s determination that NMN is excluded from the definition of a dietary supplement due to its prior investigation as a drug. The NPA argues that the FDA’s retroactive application of the law is unlawful and harms the dietary supplement industry.
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