Leader Earwax Removal Kit
Product Images NDC 70000-0490

3 FDA label images from Cardinal Health, 110 Dba Leader · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Leader Earwax Removal Kit (NDC 70000-0490). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Cardinal Health, 110 Dba Leader, 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

Ldrwax

Ldrwax
The packaging label for LEADER Earwax Removal Drops features the product name prominently with carbamide peroxide 6.5% as the active ingredient in a 0.5 FL OZ (15 mL) bottle. The label includes usage information, warnings, and directions, highlighting the product's function as an earwax removal aid with safe, gentle, foaming cleansing action. It is manufactured by Cardinal Health, 110 dba Leader.*
FDA Label Image

Leader2022

Leader2022
LEADER Earwax Removal Drops packaging label features the active ingredient carbamide peroxide 6.5%. The label indicates the product is an earwax removal aid in a 0.5 fl oz (15 mL) dosage form. It highlights safe and gentle foaming cleansing action and compares to Debrox Ear Drops active ingredient. Labeler is Cardinal Health, 110 dba Leader, distributed from Dublin, Ohio. The box includes directions, warnings, inactive ingredients, and a 100% money-back guarantee.*
FDA Label Image

Label (Label)

Label (Label)
Packaging label for LEADER Earwax Removal Kit containing carbamide peroxide 6.5% as an earwax removal aid. The kit includes 1 rubber bulb syringe and 0.5 fl oz (15 mL) of drops. Label highlights safe and gentle foaming cleansing action and compares the product to Debrox ear drops. Labeler is Cardinal Health, 110 dba Leader. The label also displays Drug Facts, usage directions, warnings, inactive ingredients, and product NDC 70000-0490.*

* 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.