E-Cig Wins Second Legal Battle With FDA
The FDA has decided to appeal the final decision of the U.S. District Court which ruled they have no jurisdiction over the sales of the e-cig. The District Court ruled that since the newest stop smoking product isn’t deemed a medicinal therapy, the FDA lacks the authority to regulate and control them. The FDA has taken issue concerning the Court’s ruling despite the fact they agree the Electronic Cigarette would in fact be valuable for smokers wanting to give up smoking cigarettes just as methadone helps opioid addicts with their dependence.
For anyone unfamiliar with this new product, it has grown into the most innovative smoking cessation product since the introduction of NRT (nicotine renewal therapies). It is a battery run device which was engineered to completely look like a cigarette. As soon as the user inhales a breath from the unit, it gives off a little shot of water vapor containing exclusively nicotine. These devices are refillable as well as rechargeable making them a lot less expensive than using tobacco. One of the benefits about their design is the fact that the nicotine refills can be bought in several strengths from 100 mg to zero mg nicotine allowing the smoker to over time taper off nicotine without having withdrawal discomforts.
Tobacco users spend upwards of $1.3 billion dollars every year on smoking cessation products. Add in the $30 billion per year smokers invest in cigarettes and you’ll see how manipulating the smoke free cigarette industry might well be driven by more than the Food & Drug Administration’s interest in the health and safety concerning US citizens. People that use the e-cig recognize this ulterior motive and have turned into a fierce and powerful group that insist the FDA recognize e-smokes as being a safe replacement for using tobacco. Opponents of the ecigarette, such as ALA (American Lung Association) and Food & Drug Administration, want them restricted until their safety can be confirmed.
The FDA has tried in the past to get regulation of the electronic cigarette. Their first attempt was noting a currently debunked analysis making claims the nicotine solution used to re-fill the electronic cigarette contained unsafe contaminants. Research paid for by a major e cig company has since identified the Food & Drug Administration’s analysis applied flawed scientific investigation procedures and thus is invalid. At this point, the ruling against the FDA’s declaration that smokeless cigarettes are medicinal products appears to be yet another nail in the coffin of the Food and Drug Administration’s attempt to control them.
There are unquestionably some unknowns linked to the ecig for instance the long term effects of their use. However the fact remains, they are certainly a significantly better option to smoking. Instead of the Food and Drug Administration wasting tens of millions of taxpayer dollars on court costs to get control of the e cig, maybe they should begin a comprehensive examination of their health impact. That is if, of course, they are genuinely interested in the health of electric cigarette users.
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