Overview

• Church & Dwight Co. filed a voluntary recall notice with the U.S. Food and Drug Administration on June 6 covering all lots within expiry of Zicam Cold Remedy Nasal Swabs, Zicam Nasal AllClear Swabs and Orajel Baby Teething Swabs
• The recall follows FDA findings that fungi may be present in the cotton tip components of the nasal and teething swabs
• Recalled products were distributed throughout the United States and Puerto Rico, and the FDA reports no serious adverse events to date
• Consumers are urged to immediately stop using the affected swabs and can obtain full refunds by visiting Church & Dwight’s website or calling 800-981-4710
• The action applies only to the specified Zicam and Orajel swab items and does not affect other products in those brands