Anybody else want to kick this guy's (Taieb's) rump?
OK, I had just made a post, but realized that I wasn't logged in and lost it. I just have a question about this all coming down to a pharmaceutical product.
Suppose that the dust all settles and we are now under the watchful eye of the FDA and using our pharmaceutical products. Could these be OTC like patches, gum, and lozenges? I assume yes but regulated as such, which has come to make some sense. (Don't kill me for saying that. There's a different story in that, entirely.)
The real question I am looking at is . . . "Who will represent "us" when the FDA starts to set limitations on flavor, concentration, and quantity?" In the worst-case scenario, based on, say lozenges: they will set tobacco, menthol, cherry, and flavorless - or something like that - then they will want anything higher than 4mg concentration to be a prescription. Since lozenges are in 72 packs, that will probably be the FDA's package size basis. Based on some suppliers' overly exaggerated claims, we'll probably be looking at 3ml bottles for purchase. Do we currently have a group that can debate with the FDA to set reasonable limits, or will they look at industry standards (LOL)?
Ya that's kinda where the problem is.
If the FDA regulates as a drug, then it will cut the Chinese, and any American operation out of the hardware or juice business. If it's regulated as a tobacco product then flavors will mostly go out the window under the same regulation as tobacco.
I'm not sure most people realize this. If the sledgehammer falls in either of those two categories, it will either be the tobacco companies who are the manufacturers, or the pharmaceutical companies. It will kill american operation, essentially, of any imported or domestic manufacturer of juice or hardware.
The action against Johnson Creek was more of a warning shot. The question as to how the FDA can legally regulate e-cigs is up in the air and undetermined. It's also important to realize that the claims that the FDA made about these vendors, are in the form of "Throw a lot of stuff at the wall and see what sticks". Just like a criminal prosecutor... because they know they will be challenged in court. I bet the FDA, includes the evidence that *customers* claimed they got off of cigarettes from the Johnson Creek website in it's amended filings. If they haven't already.
One of the other companies was putting non FDA approved erectile dysfunction drugs in their juice- a clear violation if there ever was one. I bet that this Also gets entered into evidence. Whether the amount of the drug in the juice was significant enough to actually have an effect, is irrelevant to the FDA. Right now they are looking for *press* and popular support.
What it boils down to is anti smoking hysteria, now aimed at e-cigs. And magnified by the fear that "vaping", as a smoking substitute is actually safer, thus negating the work of the anti smoking lobby- who simply hate smokers... aside form any valid points about second hand smoke and personal health. Those are only justifications.
There might also be some prejudice against "addicts" as well.
So while carping about what's in the juice might be a valid point- it may not be. We may lose this one. Right now our future rests with Njoy, and any of the american companies that may grow large enough to make a challenge- and that probably means Johnson Creek.
Think about that. Njoy and Johnson Creek. We rise and fall on what those companies are able to pull off.
Personally, I think the industry has shown a lot more responsibility than the tobacco companies ever have. And I'm good with that. I think the bigger issue is whether we have a juice industry at all.
Has anyone asked themselves why there is no USA made vaping hardware (outside of battery tubes)?
It's because no one wants to invest in the manufacturing capacity and then be closed down. Juice providers on the other hand, even doing it right, can start up for far far less.