Bidi Vapor is pushing for a ban on the marketing and distribution of synthetic nicotine
Bidi Vapor appears to be betting that a ban on Synthetic Nicotine pouches will benefit sales of its tobacco-derived nicotine pouch, which will be subject to the FDA premarket tobacco product application (PMTA) process before it can be distributed in the U.S. The reviewing process will further delay the launch of the tobacco-derived nicotine pouch, which had already been postponed due to Covid-19, according to Bidi Vapor.
Bidi Vapor is pushing for a ban on the marketing and distribution of Synthetic Nicotine in the United States, the company’s exclusive distributor, Kaival Brands Innovations Group, reported in a press release. The company, which manufactures a Synthetic Nicotine-based smokeless pouch, insists Synthetic Nicotine should be classified as an unapproved drug and thus be subject to applicable Food and Drug Administration drug regulations.
Following the FDA’s rejection of numerous PMTAs earlier this month, many companies have set their sights on Synthetic Nicotine, a legal gray area. The FDA defines a “tobacco product” as anything “made or derived from tobacco that is intended for human consumption, including any component, part or accessory of a tobacco product”—a position suggesting that Synthetic Nicotine remains outside its remit.
Conversely, we believe that many other ENDS manufacturers are utilizing Synthetic Nicotine as a loophole to avoid the rigorous PMTA process and that if Synthetic Nicotine is deemed to be an unapproved drug, the FDA will need to regulate synthetic nicotine products as unapproved drugs or remove them from the market in order to enforce and bolster compliance requirements.”
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