Otix Ear Wax Removal System Ear Wax And Bulb Kit
Product Images NDC 15579-839

Product Visual Gallery

This gallery contains 1 technical images submitted to the FDA as part of the official labeling for Otix Ear Wax Removal System Ear Wax And Bulb (NDC 15579-839). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Bell Pharmaceuticals, Inc., these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

FDA Label Image

Kit (Kit)

This product is an ear wax removal aid containing 6.5% Carbamide peroxide. It is intended to soften and remove excessive ear wax. The product should be used in the ear only and not be used if the patient has ear drainage or discharge, ear pain, irritation, rash in the ear, dizziness, ear drum injury, or perforation. The drug facts and directions are provided for individuals over 12 years of age, but children under 12 years of age should consult a doctor before use. The product should be used within 4 days, and excessive ear wax remaining should be gently flushed out with warm water. The product should be stored in its outer carton and kept away from direct sunlight. Any questions about using the product should be directed to 1-800-328-5890. This product is not a product of Prestige Brands Inc., the owner of the registered trademark Debrox®.*

* About these descriptions: Image descriptions on this page are generated by automated AI analysis of the product label images from the manufacturer's FDA label submission (SPL). They are provided for reference only and may contain errors or omissions. Always rely on the printed label itself and the official FDA labeling, and consult a pharmacist or healthcare professional with any questions about this product.