This is not the first time the public health service has felt that the FDA must crack down on synthetic nicotine
CTFK first sent a letter to FDA in 2018 to reply to the marketing promotion of Next Generation Labs, a nicotine dealer. The Next Generation Labs did not reply to the evaluation requirements of time.
In the same year, several defense lawyers dedicated to public health services fabricated lies in the Boston University Law and regulation review article. The FDA has opened a system loophole that companies can use to avoid control and can and should deal with this problem according to the control of Synthetic Nicotine products as drugs.
Neither of the two letters did much. In March 2021, the Wall Street Journal reported that puff bar, which produces a series of fashionable disposable seasoning e-cigarettes, had applied Synthetic Nicotine to avoid organizational control, which caused another letter from CTFK and other physical and mental health institutions to FDA.
Abboud, who comes from the steam technology research association, said he was afraid that if the FDA controlled Synthetic Nicotine as a drug, many e-cigarette companies would go bankrupt and might return the sales market to traditional tobacco companies. Compared with all other control methods, drug licensing methods are more complex, time-consuming and even more expensive.
This may be true. However, Henigan of CTFK shows that it is impossible for the company to market only the equipment they feel suitable for. This kind of company is realized under the assumption that they will not be controlled at all, which is a dangerous situation.
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