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  2. Premarket tobacco application - Wikipedia

    en.wikipedia.org/wiki/Premarket_tobacco_application

    On May 10, 2016, the US FDA finalized its "deeming" rule, subjecting additional products to scrutiny under the Federal Food, Drug and Cosmetic Act as amended by the Family Smoking Prevention and Tobacco Control Act. [4] The rule gives the US FDA authority to regulate e-cigarettes, cigars, and vape pens.

  3. ‘You’re failing!’: the federal government is having a ...

    www.aol.com/finance/failing-federal-government...

    To date, the FDA has issued a number of warning letters to domestic manufacturers of vapes, in addition to the import bans. However, the inclusion of the U.S. Postal Inspection Service in the new ...

  4. Vaporizer (inhalation device) - Wikipedia

    en.wikipedia.org/wiki/Vaporizer_(inhalation_device)

    This is an accepted version of this page This is the latest accepted revision, reviewed on 25 January 2025. Device to vaporize substances for inhalation A vaporization heat wand and vaporization chamber bowl used to deliver vapor through a water pipe A vaporizer or vaporiser, colloquially known as a vape, is a device used to vaporize substances for inhalation. Plant substances can be used ...

  5. Regulation of electronic cigarettes - Wikipedia

    en.wikipedia.org/wiki/Regulation_of_electronic...

    Therapeutic vapes with a nicotine concentration of 20 mg/mL or less are available from a pharmacy to anyone 18 years or older subject to a pharmacists approval. Therapeutic vapes with a nicotine concentration greater than 20 mg/mL or for anyone under 18 require a prescription. [168] Australia is developing regulations on e-cigarettes. [169]

  6. In a first, FDA authorizes flavored vape products from Altria ...

    www.aol.com/news/first-fda-authorizes-flavored-e...

    (Reuters) -The U.S. Food and Drug Administration authorized four of Altria's menthol e-cigarette products for sale in the country on Friday, making them the first ever flavored vapes the agency ...

  7. FDA ordered to reconsider denial of approval for vape products

    www.aol.com/news/fda-ordered-reconsider-denial...

    A federal appeals court on Wednesday ordered the U.S. Food and Drug Administration to reconsider its decision barring two makers of flavored liquid for e-cigarettes from marketing their products ...

  8. The FDA reverses ban on Juul e-cigarettes - AOL

    www.aol.com/news/fda-reverses-ban-juul-e...

    The Food and Drug Administration announced Thursday that it has reversed its ban on Juul e-cigarettes while it reviews new court decisions and considers updated information provided by the vape maker.

  9. Approved Drug Products with Therapeutic Equivalence ...

    en.wikipedia.org/wiki/Approved_Drug_Products...

    Approved Drug Products with Therapeutic Equivalence Evaluations, commonly known as the Orange Book, is a publication produced by the United States Food and Drug Administration (FDA), as required by the Drug Price and Competition Act (Hatch-Waxman Act). The Hatch-Waxman Act was created to '"strike a balance between two competing policy interests: