Wow, that seems way over the top to me, willpower.
Plus, it is only
arguable that ecigs fall within the Food and Drug Act definition of a drug or drug device. Just because someone at the FDA has declared it so does not make it so. Federal agencies have been shot down on their interpretation of federal statutes time and time again by the courts, just as sometimes they are upheld in their interpretations.
Thus, whether or not ecigs or the liquids alone are actually "illegal" ultimately remains to be seen, and this issue probably has to be decided in a court of law if not resolved to everyone's satisfaction short of litigation.
Oh, by the way you cited the wrong section of the law. As you can see from the FDA letter posted here,
http://www.e-cigarette-forum.com/fo...-important-email-fda-supplier.html#post173081,
the relevant sections of the Food and Drug Act are:
"503(g)(1) of the Federal Food, Drug, and Cosmetic Act (the Act) (21 U.S.C. 353(g)(1)) with their "drug" uses, as defined by section 201(g) of the Act (21 U.S.C. § 321(g))".
For the crucial definition of a drug and drug device (201(g)), you can see the actual text of the statute here:
Yes. I understand. That's why I said "section 505 and other provisions therein (of FDCA)". 505 defines the New Drug Application (NDA) requirements along prohibition of introduction of new drug without NDA requirements. Technically, I see it as more of violation of 505, the prohibition, not a violation of drug definition. But, I do see you point.
Litigation is interesting. Granted, some vendors sanitized their website a lot like PS, making it different for FDA. Here is the thing:
FDA is going case-by-case. Most of them don't have enough capital to do protracted litigation with FDA. They will fold. How about class action? Judge won't certify your class, because FDA is claiming that each case is different and that's why they investigated case-by-case.
Let's for some wild luck, you got your class certified by the court. Great? Yeah now, it's a winner-take-all or all-in situation (win or lose all together). Since you claimed that you are a single class, FDA will go after the worst offender to make their case.
Let's say everything worked by some miracle. What's the defense here? We have nicotine, but it's not nicotine replacement; it is a nicotine supplement, just in case people did get enough nic from cigarettes? Or should we claim that it is for hooking non-smokers to nicotine? Neither sounds good. Our dilemma.
In addition, here is a real Perry Mason moment for you:
"Mr. Supplier, you claim that your product is not NRT, hence not subject to DNA provision of FDCA. To your best knowledge, have you or any of your co-respondents gone onto a public forum known as ECF and ask your customers send to letters to senators telling them how they wonderfully transform their lives by quitting smoking with help of you product?"
"YES"
Just in case not clear, our Plan B is vitiating the validity of argument in Plan A. We can't ask senators to keep e-cigs on the market because of the drug benefits, then go to the court and claim that e-cigs should not be under FDA jurisdiction because they are not drug. Probably first-year law student would tear us into bits.
Besides, to my knowledge there is NO product with nicotine (for human consumption) that had any decent level of acceptance among public were not classifed as drug in court or FDA.
My 2 cents on the "it is not a drug" approach.