New MS Guidelines, Zyn's FDA Claim and Norovirus Warnings
14 Articles
14 Articles
Health expert discusses nicotine pouch risks following FDA marketing ruling
Following the U.S. Food and Drug Administration’s recent authorization for Swedish Match USA, Inc. to market ZYN nicotine pouches with a modified risk claim, a local tobacco treatment specialist is warning that the products still have their drawbacks.
USA/Tobacco: Philip Morris Authorized to Report Reduced Risk in Nicotine Bags ZYN Against Cigarettes
The Food and Drug Administration (FDA) of the United States has authorized the marketing of 20 variants of ZYN nicotine bags with claims of reduced health risk to traditional cigarettes, announced to Philip Morris International (PMI). According to the statement of the multinational, owner of the Portuguese company Tabaqueira, this decision under the Modified Risk Tobacco Product (MRTP) regime constitutes the first authorization of the genus gran…
Philip Morris claims FDA nod to market ZYN nicotine pouch as safer than smoking
The FDA has authorized Philip Morris International's ZYN nicotine pouches for reduced-risk marketing. This marks the first such approval for a nicotine pouch product in the United States. The regulator concluded ZYN could significantly reduce harm compared to cigarette smoking. This decision allows adult nicotine users access to science-based health information. The authorization applies to specific marketing claims and authorized ZYN products.
By this decision, ZYN becomes the first product in the nicotine envelope category to receive such authorisation, which allows...
The FDA Is Finally Following Its Own Science on Harm Reduction
Now that Marty Makary has departed as Food and Drug Administration (FDA) Commissioner, the agency he left behind is turning the page on his disappointing legacy. In May, while Makary was still in post, the FDA authorized four vaping products from Glas Inc.—including the first fruit flavors, mango and blueberry, ever to clear its review […]
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