Earclearrx
Product Images NDC 74318-102

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 1 technical images submitted to the FDA as part of the official labeling for Earclearrx (NDC 74318-102). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Nuance Medical, Llc, 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

Principal Display Panel (15 mL Bottle Label)

Principal Display Panel (15 mL Bottle Label)
Earclear & Ear Wax Removal Drops contain Carbamide Peroxide USP 6.5% as an active ingredient. These drops are used occasionally to soften, loosen, and remove excessive earwax. The product is warned to be used only under the guidance of a doctor in case of ear drainage, discharge, pain, irritation, dizziness, injury, or perforation of the eardrum. The drops are only for use in the ear, and it can lead to side-effects if it comes in contact with the eyes. The product is only to be used for four days, and if needed more, consult a doctor. The product should be kept out of the reach of children, and if swallowed, medical help is to be sought. The inactive ingredients include glycerin, propylene glycol, sodium bicarbonate, lactic acid, and purified water. The product should not be stored above 77°F. The product is distributed by Nuance Medical LLC and made in the USA.*

* 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.