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For more on the FDAs premarket review process for e-cigarettes, see the Public Health Law Centers factsheet, Extensions and Epidemics: The FDAs Gatekeeping Authority for E-Cigarettes and see updates on the FDA decisions on their Tobacco Product Applications: Metrics & Reporting page as well as on their Tobacco Product Marketing Orders page

The descriptor change occurred because the FDA banned product descriptors such as "Light," "Ultra Light" and "Mild" in 2010

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