There may be an easy answer to the FDA ban in Electronic Cigarette News; Originally Posted by rlorange
I think trial and error with the solvent used to extract the nicotine from the patch ...
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Originally Posted by
rlorange
I think trial and error with the solvent used to extract the nicotine from the patch plus filtering should get rid of any glue. Find the solvent which leaves the glue alone yet still dissolves nicotine. I'm guessing the most polar one because the glue resists water, maybe methanol.
put the nic' crystals in a bowl, pour in acetone, knead the crystals to remove the glue(glue will go into acetone) poor out acetone, rinse and repeat 5 times, I use to do illegal things
, this is how u get the glue out. acetone is fingernail polish remover, fingernail polish is "glued" to your fingernails.
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Home "Nicotine Recycling" ?!?!
Ok, I've held my tongue 'til now, But some of you folks appear to be seriously considering an attempt at recycling/extracting nicotine in your homes.... Please, do not ever attempt any off-handed ideas that you find anywhere on the internet as a means of extracting or concentrating nicotine! Especially with the intent of using the material for human ingestion!
The health and safety risks are far greater than people seem to realize here and I'd hate to see a post titled "E-Vaper123 found dead" posted by a family member, trying to learn why their relative appeared to be running a Meth lab in his kitchen.
I have personally worked with concentrated Nicotine (By the Drum) in the past, Let me assure you.. It is not just a possibility you will harm or kill yourself... It is Very likely!!!
Mike
Last edited by StratOvation; 03-15-2009 at 04:01 PM.
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FDA has my juice!
The FDA has my juice and are asking for a drug listing number. I understand from discussions that the nicotine levels are not high enough for there to be a drug listing number and therefor the FDA to be involved until they make a ruling accross the board.
Anyone know what I should tell them besides threatening to sue in order to get my juice? HELP! I need my juice!
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The FDA have categorised eliquid as a drug, they haven't specified nicotine levels that might be acceptable. The UK Trading Standards have assessed eliquid under the Poisons Act and found that no restrictions apply because nicotine concentration is not high enough. Maybe you're getting US and UK enforcement mixed up.
Some shipments have been returned to sender from US customs because eliquid is not approved.
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Originally Posted by
sleets1
The
FDA has my juice and are asking for a drug listing number. I understand from discussions that the nicotine levels are not high enough for there to be a drug listing number and therefor the
FDA to be involved until they make a ruling accross the board.
Anyone know what I should tell them besides threatening to sue in order to get my juice? HELP! I need my juice!
As I understand it Sleets.... The FDA is asking you for a number that does not yet exist because they haven't issued a number for "Nicotine in a PG solution". To date the FDA has reffered to your juice only as a "New Drug".
Obviously..."New non-approved" drugs do not have a FDA listing number.
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There was another report of seized liquid where the FDA wanted an "NDA" number for the liquid. That's new drug approval. And there isn't one. You might have to kiss that liquid goodbye. Keep us posted on the ultimate outcome. We had one poster like this ... many posts followed .. and the original guy never told us how it turned out.
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Sleets,
My response to your earlier post was a bit rushed...I'm curious what the vaue of "Your Juice" is, Primarily for one reason...unless you have several thousands of dollars wrapped up in this particular shipment...take TB's advice and write it off...consider it a loss and try to continue with doing business.
I've dealt directly with many FDA field auditors over a couple of decades +, One thing I can say as an absolute....Never, ever, under any circumstance is it a wise move to threaten the FDA with legal action unless you have previously consulted with your legal team and gained their whole hearted support and confidence that you have a solid case.
And if you are able to garner the full support of your legal staff.....Start looking for a new legal staff, because you probably have a stable full of nags that cannot finish this sorta race.
We (Distributors, Suppliers and end use consumers) all have to prepare for what is likely to be a challenging and protracted uphill battle to maintain some semblance of a viable US market for the foreseeable future.
Mike
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Thanks for the replies fellows. Four of us got together to try and get in on discounted juice before the crackdown happened. We don't have a lot of money invested but we wanted a years worth for all four of us.
I spoke with the UPS agent attached to the FDA and have a call in to the FDA and was basically told that NO shipments were being cleared for any reason and what are our intentions concerning the juice. Choices were to have it destroyed or shipped back to the manufacturer.
Not enough $$ involved to fight it but am willing to do my part. Not sure what that is at this point
Vape on!
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Perhaps it's time to start passing around the hat get a fund together to pay researchers and lawyers to act on our behalf. But sitting around and complaining will not get stuff though the approval process. While it may seem daunting, the main ingredients are pretty well known so it wouldn't be like getting approval for a new drug.
I think it's also time that we start putting pressure on retailers making medical or safety claims. Even one or two bad retailers will give them the bait they need to streamroll the rest.
Last edited by ratfink; 03-25-2009 at 12:01 PM.
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Originally Posted by
bizzyb0t
That doesn't make any sense! They haven't banned "water tobacco pipes", other glass pipes. Those are all used for much more than tobacco. There's vaporizers (much larger than the e-cig) used to smoke weed. Those haven't been banned yet and most likely will never be banned. I don't see how the e-cig hardware could ever be deemed illegal.
The water is a bit murky here. The FDA can limit sales on "Medical Devices" if they deem it so and has 3 classes of increasing regulation. But even making the devices a Class I device could require FDA oversight at the factories, mandatory labeling requirements and registration.
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