Synthetic nicotine is likely to be officially regulated by FDA
At present, the U.S. Congress has a pending proposal to incorporate Synthetic Nicotine into the terms of reference of the FDA tobacco Department, which seems very likely to be passed. Before the change of FDA’s terms of reference, the most important significance of dealing with products using Synthetic Nicotine on a case by case basis is to avoid misleading consumers caused by false publicity.
For example, the left-handed purification of some Synthetic Nicotine has not been completed, which may mislead users in the identification of product concentration. Assuming that he actually uses raw materials containing 1:1 L-D nicotine, only 50% of nicotine can relieve users’ addiction.
The manufacturer may only label the amount of “effective” nicotine (i.e. S-nicotine) in order not to make the product appear to contain ultra-high concentration of nicotine, but the user actually inhaled twice the amount marked. Another point worth noting is that nicotine, as a psychoactive compound, the Drug Department of FDA has the right to control and implement the supervision and disposal of products containing Synthetic Nicotine.
Even if the tobacco department does not inspect and handle some Synthetic Nicotine products that bypass PMTA temporarily, the local office of the drug department can also implement it from the perspective of drug production and supervision, which will generally be more strict.
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