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But the Food & Drug Administration is still, as Time.com recently put it, is dragging its feet on regulating the $2 billion industry

The applications for these products did not present sufficient scientific evidence to show that the potential benefit to adult smokers outweighs the risks of youth initiation and use. When reviewing premarket tobacco product applications (PMTAs), the agency evaluates, among other things, a tobacco products components, ingredients, additives, constituents, design, harmful and potentially harmful constituents and health risks, as well as how the product is manufactured, packaged and labeled

If left untreated, these diseases can lead to irreversible vision loss and possible blindness

Within a few minutes, I felt a slight buzz from all those ingredients, and I took another hit