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Source: TOBACCO REPORTER, 6/13/22
A coalition of more than 30 U.S. attorneys general have called on the U.S. Food and Drug Administration to reject marketing authorization for all nontobacco nicotine products, which they say are currently being sold without regulation of their contents, manufacturing, health effects, required warning labels or marketing claims. In a letter directed to FDA Commissioner Robert Califf, the coalition argues that these products currently don’t meet the FDA’s public health standard... For more of this story, click here.
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