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The FDA's January 2026 review of ZYN's modified-risk application included explicit consideration of youth exposure to reduced-risk messaging, with the agency noting that claim exposure did not increase use intentions among young adults but requiring ongoing post-market surveillance to detect unintended uptake [2]Source: Food and Drug Administration, "Meeting of the Tobacco Products Scientific Advisory Committee (TPSAC)", fda.gov

FDA, NIH, and other federal agencies should also identify strategies for tracking these activities, especially those that appeal to youth