Ear Wax Removal Drops
Product Images NDC 50804-341

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Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Ear Wax Removal Drops (NDC 50804-341). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Goodsense, 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 (Carton label 0.5 FLOZ)

Principal Display Panel (Carton label 0.5 FLOZ)
This is a drug facts sheet for ear wax removal drops containing 6.5% carbamide peroxide. Its purpose is to soften, loosen, and remove excessive ear wax. It is essential to avoid contact with the eyes and consult a doctor before use if there is ear drainage or discharge, ear pain, irritation or rash in the ear, dizziness, an injury or perforation of the eardrum, or recent ear surgery. It is for occasional use and should not be used for more than four days. The product foams on contact with ear wax, and there may be a "crackling" sound. It is registered as GoodSense, manufactured and distributed by Direct Perrigo, Inc. It is not available for storage above 77°F (25°C) and should be kept in the outer carton. If swallowed, it is essential to seek immediate medical help or a Poison Control Center. The bottle contains 0.5FLOZ (15 mL) with an actual size of 8 | 46036 5514 0017.*
FDA Label Image

Principal Display Panel (Carton label KIT 0.5 FL OZ)

Principal Display Panel (Carton label KIT 0.5 FL OZ)
This is a warning label for an ear cleaning product. It advises users to consult a doctor before use if they have ear drainage, injury or perforation of the eardrum, or recent ear surgery. The product should not come in contact with the eyes, and if used for more than four days, users should consult a doctor. It contains citric acid, glycerin, propylene glycol, sodium citrate, sodium lauryl sulfate, and tartaric acid. The kit includes a soft rubber bulb ear syringe and drops, and it is produced by a company located in Georgia.*
FDA Label Image

Principal Display Panel Bottle Label 0.5 Fl Oz (790866 Good Sense Ear Wax Drops Label)

* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.