Everyone on this forum needs to chill. The only reason that e-cigarettes would need approval from the FDA is to be able to legally market the product as healthier or as a cessation method...
...E-cigs are here to stay, and the FDA has no jurisdiction to do anything about it.
I would hope that your beliefs are valid but I can't be so sure. I came accross this piece recently: http://www.naturalnews.com/025606.html
The FDA has effectively banned a naturally-occurring form of vitamin B6 called pyridoxamine by declaring it to be a drug, reports the American Association for Health Freedom. Responding to a petition filed by a drug company, the FDA declared pyridoxamine to be "a new drug."
Now, any nutritional supplements containing pyridoxamine will be considered adulterated and illegal by the FDA, which may raid vitamin companies and seize such products. See the history of FDA raids on vitamin companies here: http://www.naturalnews.com/021791.html
Pyridoxamine occurs naturally in fish, chicken and other foods (http://en.wikipedia.org/wiki/Vitamin_B6), putting the FDA in the strange position of banning a substance from dietary supplements even though it is already present in the food supply.
It's not the first time the FDA has declared a natural molecule to be a "drug" while attacking nutritional supplements that contain the same molecule. A similar story unfolded with red yeast rice and the lovastatin molecules it contains that lower high cholesterol. The drug companies engaged in biopiracy, ripping off the molecule from red yeast rice to make their now-famous "statin drugs." Once the statin drugs were patented, Big Pharma and the FDA went after red yeast rice, claiming the supplement was "adulterated with pharmaceuticals."
Now on the the website that lists Refusal Actions by FDA as Recorded in OASIS - the reason given for the refusal for some consignments of electronic cigarettes is that they are both "unapproved" and "not listed".
Unapproved means that it is seen by the FDA as a 'new drug'. Do you think that this is because the box/manual of this devices, some of which were from the popular Joye manufacturer, had cessation device labels or made health claims? and that as long boxes are not marked as such then users in the US will be able to circumvent the FDA?
Judging not least by the letter federal scientists working at the FDA recently sent to Obama accusing the FDA of being corrupted, It seems that the FDA have largely been able to get away with whatever they have wanted in the past and the health and welfare of the citizens of the US is not always the key motive or a priority for their decisions and that the generous hand of Big Pharm has a presence in their ranks.
I fear If the FDA want these banned they'll find a reason to make it so and no amount of angry letters to .gov will change that course of action. Labelling them as cessation devices or making 'healthy' claims just spurs the process.
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