Believe me, i'm not arguing over the newness of the argument, or lack thereof, just over why the
FDA suddenly decided to get involved. Popularity aside, The
FDA's usual stance is that a drug must be approved
before it goes to market; that did not happen with any of the tobacco companies' products because they are/were "tobacco products," outside the
FDA's jurisdiction.
If the Premier cigarette or other alternatives ever became popular, do you really think that the
FDA would suddenly decide one day that these are "drug delivery devices" in need of approval or ban and not "tobacco products" even though they clearly are?
To reiterate my original theories on why these devices are "tobacco" and e-cigs are "drugs":
I'm really banking on #3, but i do think #'s 1 and 2 play a role.
Popularity does come into play with regards to recognizing that there is a product on the market that needs to be classified legally and perhaps regulated, but why not classify it as a "tobacco product" with all the requisite health warnings and such, since it is clearly an alternative to smoking? What in the world makes something that is a smoking alternative which contains and delivers a tobacco extract NOT a tobacco product?
Phew. This is getting tough indeed.
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