DSHEA Weekly Digest – April 14, 2026
DSHEA Weekly Digest – April 14, 2026 Weekly Digest April 14, 2026 Volume 1, Issue 2 What’s Inside This Week FDA Deputy Commissioner Kyle Diamantas
April 14, 2026
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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 Weekly Digest – April 14, 2026 Weekly Digest April 14, 2026 Volume 1, Issue 2 What’s Inside This Week FDA Deputy Commissioner Kyle Diamantas
DSHEA Weekly Digest Weekly Digest March 23 – April 1, 2026 What’s Inside This Week FDA Holds Most Consequential Supplement Hearing Since DSHEA’s Passage
DSHEA Weekly Digest Weekly Digest April 7, 2026 Volume 1, Issue 1 What’s Inside This Week FDA Moves Simultaneously on DSHEA Innovation and Supplement
Congress struck a careful balance between providing consumers with access to safe dietary supplements and maintaining strict safety and efficacy standards for drugs when it
On July 21, 2025, the Orrin G. Hatch Foundation hosted a timely and important conversation on the future of the Dietary Supplement Health and Education
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
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.
...Press Release
The FDA announced that β-nicotinamide mononucleotide (β-NMN) is not a legal dietary ingredient, citing its prior investigation as a drug. The Council for Responsible Nutrition (CRN) responded, expressing concern that this decision stifles innovation and disregards consumer interests.
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