Keystone Industries — FDA Class II (D-0604-2026)

Keystone Industries is recalling 450 units of a human over-the-counter dental drug containing benzocaine due to defective containers. The recall is classified as a voluntary action. The affected product is identified by NDC 69483-001.

• •Keystone Industries is recalling 450 units of a benzocaine dental product.
• •The recall is due to defective containers that may contain faulty bottles.
• •This is a voluntary recall classified as Class II by the FDA.
• •Consumers should check their medicine cabinets for the affected product.

Consumers who purchased this dental product should verify if they have one of the 450 affected units to prevent potential health risks. The recall is a precautionary measure.