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2. Toner cartridge - Wikipedia

   en.wikipedia.org/wiki/Toner_cartridge

   Some toner cartridges incorporate the drum unit in the design, and both drum and cartridge are replaced simultaneously; cost of a cartridge is higher than a toner-only cartridge, although separate drum replacement is avoided. Toner cartridges have the same function as ink cartridges used by inkjet printers.

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

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

   Earlier this month, the FDA rescinded market denial orders issued in 2022 for four varieties of Juul Lab's tobacco and menthol-flavored pods and its e-cigarette device.

4. Toner refill - Wikipedia

   en.wikipedia.org/wiki/Toner_refill

   It is common for toner cartridges to be sold with reply paid labels enabling them to be returned to the manufacturer for recycling and reuse. Refilling and resale by a third party Many independent companies that sell toner cartridges refill and reuse the original manufacturer's cartridges which they typically obtain from recycling companies.

5. FDA Belatedly and Arbitrarily Approves Menthol Vapes

   www.aol.com/news/fdas-belated-approval-menthol...

   The agency's inscrutable approach to harm-reducing nicotine products sacrifices consumer choice and public health on the altar of youth protection.

6. 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:

7. Regulation of tobacco by the U.S. Food and Drug Administration

   en.wikipedia.org/wiki/Regulation_of_tobacco_by...

   The Family Smoking Prevention and Tobacco Control Act (also known as the FSPTC Act) was signed into law by President Barack Obama on June 22, 2009. This bill changed the scope of tobacco policy in the United States by giving the FDA the ability to regulate tobacco products, similar to how it has regulated food and pharmaceuticals since the passing of the Pure Food and Drug Act in 1906.