Wouldn't YOU if given the choice opt for the brand that was stamped "FDA APPROVED"?
You mean something like Chantix?
Wouldn't YOU if given the choice opt for the brand that was stamped "FDA APPROVED"?
Your notes on pharmaceutical grade propylene glycol and their safety history fails to mention one very important fact. NONE of the products you mention are to be inhaled directly into the lungs. This is a very different way to deliver any chemicals. There are several products that can cause a great deal of harm by intentionally inhaling them into the lungs (huffing).
You mean something like Chantix?
No.
The FDA is corrupt. Their recommendations are driven by bribes and lobbying, especially Big Pharma.
Sorry, but if the government says something, I don't put a whole lot of faith on it being accurate or reliable.
I'm pretty sure he meant no to the idea that an FDA stamp of approval means anything."No" what?
No to "the manufacturers to design and SEEK OUT APPROVAL from the FDA or ALA"
Or No to "You can't just generalise about "ecigarettes" when it comes to safety"
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2: Instead of the ALA or the FDA approving or denouncing a generality, the onus is really on the manufacturers to design and SEEK OUT APPROVAL from the FDA or ALA.
Wouldn't YOU if given the choice opt for the brand that was stamped "FDA APPROVED"?
Obviously, you don't understand the history of vaping. It appears you are suggesting that those who manufacture eliquid and vaping equipment should go through the process for FDA approval. This is exactly what the FDA wanted when they banned vaping nationwide in 2009. That would take anywhere from 10 - 20 years, cost multiple millions and still run a high risk of being banned.
We would all still be smoking if that path were followed. That's a "fools errand".
Obviously, you don't understand the history of vaping. It appears you are suggesting that those who manufacture eliquid and vaping equipment should go through the process for FDA approval. This is exactly what the FDA wanted when they banned vaping nationwide in 2009. That would take anywhere from 10 - 20 years, cost multiple millions and still run a high risk of being banned.
We would all still be smoking if that path were followed. That's a "fools errand".
You seem to be saying that SEEKING APPROVAL from the FDA means not selling product until approval.
What I'm saying is SEEK APPROVAL. If the FDA objects to use of certain materials, then redesign without those materials and SEEK APPROVAL again.
If I were a manufacturer, I'd want to get a stamp of APPROVAL on MY product to distinguish it from competition; What about USP Grade? If I could USP Grade Approval for my pyrex clearo I'd put a USP stamp on it.
The problem is right now the vaping industry is still content to align itself with junkies and "drugs" when it should be aiming for STANDARDS and QUALITY.
If I were a manufacturer, I'd want to get a stamp of APPROVAL on MY product to distinguish it from competition; What about USP Grade? If I could USP Grade Approval for my pyrex clearo I'd put a USP stamp on it.
@Masterchief68:
Somehow, it always makes me mad when FDA starts talking BS about 'their' safe (Chantix) and effective (In about 5 per cent of users) quitting methods...
With 'approved' methods doing that poorly, I would just assume it remains 'unapproved'
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Why would the industry seek approval from the body that tried to unilaterally shut it down in 2009?
When has the FDA ever demonstrated any sense of reason or logic with its treatment of vapors or vaping?
In fact, it is up to the FDA to outline the approval process before we blame manufacturers. To my knowledge, the FDA has not done so. Lets not blame our vendors for not applying yet.
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You might be interested in this then...I hope I didn't appear to be blaming manufacturers or vendors; I merely meant to say that the manufacturers should be proactive - perhaps PREEMPTIVE would be a better word, to seek approvals.
I am saying PREEMPT that.