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SpinDistribute.com Article Directory

The following article was published in our article directory on September 1, 2011.
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Regulations Settled Between FDA and E Cigarette Makers

Article Category: Recreation

Author Name: Bob Thomas

There have been attempts to regulate the imports and manufacturing since 2008 but an evident relationship between the suppliers of e cigarettes and the FDA has only recently been established. There where also concerns over advertising and public health regulation was hampered by issues regarding jurisdiction and classification.

The marketing of these goods created the impression that they where an entirely harmless alternative to smoking as the nicotine was delivered by a liquid being vaporized by a digital cigarette. There where also businesses that claimed that they could be used as a nicotine replacement for people wanting to stop smoking. Neither of these claims where supported by the FDA and they don't endorse them as a form of nicotine replacement.

There was a public warning which was sent out at press conference as a result of concerns from particular groups and tests done one e cigarette cartridges. Some people felt that they could be a risk to younger people as they could find the fruit flavors appealing and it could lead non smokers to try other tobacco products. The claims that they where entirely harmless where also uncertain when test results disclosed that they contained a carcinogen and irritants originating from tobacco.

It is in addition became apparent there ought to be more attention paid to standards of manufacturing and product labeling. Only one or more of the cartridges which where meant to be nicotine free actually had no nicotine when tested and cartridges which where meant to deliver specified amounts of nicotine did not emit the same amount consistently.

The food and drug administration announced in September 2010 that it had taken action against five businesses who where in contravention with the Federal Food, Drug and Cosmetic Act (FDCA). These businesses had either made unsubstantiated claims or there manufacturing practices where lower than standard. Some claimed that e cigarettes maybe used as a nicotine replacement when giving up smoking which is a medical claim. One company even claimed that its products maybe employed for weight reduction or erectile dysfunction.

Before this even the food and drug administration had attempted to stop the import of e cigarettes because they had classified them as a drug and shipping device combination. It didn't stop the sale of merchandises and one or more of the companies which was dependent on their products being denied entry took the case to court. Their argument was that they could not be classified as drug shipping devices if they where not sold as an item with any therapeutic benefit.

The courts eventually ruled in their favor but during the trial a new legislation was enacted which gave jurisdiction over tobacco products and even products derived from tobacco to the food and drug administration. This finally allowed them to have control of the issues that where of concern and there might be restrictions placed on things such as marketing. E cigarettes could not be advertized alongside other products that are regulated for example. The normal of manufacturing could easily now be regulated.

A pre market review is now also required before new products can enter the market unless they have been sold since before February 2007 and have not been modified since. Products that are promoted as having any therapeutic benefit will still be dependent on medical classification but regulation guidelines have not yet been stipulated. If anything product will now be able to be sold more freely now that there is a firm understanding between makers of e cigarettes and the FDA.

Keywords: e cigarette, electronic cigarette, electric cigarette, vapor cigarettes, smokeless cigarettes

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