Lacey, I agree with your last post, but with one small exception. The legislation that just passed in the Senate is squarely directed at "tobacco" products, not at nicotine per se. The FDA has always had jurisdiction over nicotine-based smoking cessation products, as they are undisputedly drugs.
Our ecigs are still in that gray area, with their classification for legal purposes yet to be finally resolved, I think.
Yes. I can agree with this.
I say that they will attempt to control all nicotine because the average citizen will not be able to understand that nicotine and tobacco are not one in the same. In essence, I think the FDA will try to pull the same stuff they did in the late 1990's when they ended up in court regarding tobacco. They have a ton of pressure from the pharmaceutical funded anti-smoking groups to bannish the ecig from American soil forever.
It will be an expensive fight, but we just need to buy some time... get more people (doctors and journalists) the ability to see the positives and get behind this as a true revolution in tobacco harm reduction. It also allows us smaller companies some time to get some funding together and provide our own tests on our own products.
I think the ecig falls into a grey area because of suppliers who do not make smoking cessation claims. Those who make claims, will be the first ones that the FDA comes after once they do decide to crack down. Warnings have been given now for some time that health and safety claims are in fact FDA jurisdiction and you do have to prove them with proper testing and trials.
The only products that have been classified or noted as a "new drug" or a "medical device" are those products that make "health", "safety" or "cessation" claims, or were mis-marked on entry, or some customs agent went above and beyond their authority for whatever reason.