Breaking News Canesten Extra Spray Recalled Due To Active Ingredient Concerns

Breaking News: Canesten Extra Spray Recalled Due to Active Ingredient Concerns

Canesten Dermatological Spray Recalled, Alternative Treatments Available

The U.S. Food and Drug Administration (FDA) has announced the recall of Canesten Extra Spray due to concerns about the active ingredient, Bifonazole. Bifonazole has been linked to rare but potentially serious side effects, including liver damage and kidney failure.

Canesten Dermatological Spray Recall Details

The recalled product is Canesten Extra Spray, a topical antifungal medication used to treat skin infections such as athlete's foot and jock itch. The product is available in 1-ounce bottles and is packaged in a white and blue box with the words "Canesten Extra Spray" prominently displayed. The recall affects all lots of the product.

Consumers Advised to Stop Using Canesten Extra Spray

Consumers who have purchased Canesten Extra Spray are advised to stop using the product immediately. The FDA recommends consulting with a healthcare professional for alternative treatment options.


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