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Eye ointments sold at CVS and Walmart may not actually be sterile, a recall posted by the US Food and Drug Administration warned. On Feb. 26, the FDA posted a voluntary recall from Brassica Pharma ...
Clear Eyes Once Daily, Eye Allergy Itch Relief: Not officially linked to any bacterial infection cases being traced by the CDC, the FDA has indicated this brand's manufacturer, Teva ...
Doxylamine alone is available over-the-counter, whereas doxylamine in combination with pyridoxine is a prescription-only medication. [22] Doxylamine is also available in over-the-counter nighttime cold medicine products such as NyQuil Cold & Flu (contains acetaminophen , doxylamine succinate 6.25 to 12.5 mg, and dextromethorphan hydrobromide ...
The FDA posting of the recall says Teva’s pulling Clear Eyes, Once Daily, Eye Allergy Itch Relief drops for a failed impurities test. This covers the 715,682 bottles in lot Nos. 114349 ...
The 2022–2023 United States Pseudomonas aeruginosa outbreak began in May 2022, with the infection of several patients in California. The Centers for Disease Control and Prevention (CDC) became aware of a strain of Pseudomonas aeruginosa in artificial tears manufactured by EzriCare and Delsam Pharma in January 2023.
Drugs or medicines may be withdrawn from commercial markets because of risks to patients, but also because of commercial reasons (e.g. lack of demand and relatively high production costs).
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A drug recall removes a prescription or over-the-counter drug from the market. Drug recalls in the United States are made by the FDA or the creators of the drug when certain criteria are met. When a drug recall is made, the drug is removed from the market and potential legal action can be taken depending on the severity of the drug recall. [1]