Earwax Removal Drops Liquid
Product Images NDC 52412-600

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This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Earwax Removal Drops (NDC 52412-600). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

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

Product Images & Figures Index

FDA Label Image

Ero Ifc.jpg (Ero Ifc)

Ero Ifc.jpg (Ero Ifc)
Not available. The provided text seems to be an unpredictable combination of garbled characters, symbols, and numbers that do not form a coherent and understandable description.*
FDA Label Image

Ero Label

Ero Label
This product is earwax removal drops with chamomile and aloe. It is cautioned that the tamper evidence shrink film should not be broken or missing. Users are advised to ask a doctor before use if they have ear drainage or discharge, pain, irritation or rash in the ear, dizziness, or an injury or perforation of the eardrum, or if they have recently had ear surgery. The product should be kept out of reach of children, and users are cautioned not to use it excessively or for more than four days. It is also advised to avoid contact with the eyes, and users are cautioned that the product is not intended to restore hearing loss due to medical reasons. The product contains 0.5 FL OZ (15 mL) and has an active ingredient of carbamide peroxide 6.5%. Users over 12 years of age can take 5 to 10 drops in the ear for several minutes. If needed, it can be used twice daily for up to four days, or as directed by a doctor. Any wax remaining after treatment may be removed by gently flushing the ear with warm water using an ear bulb syringe. Children under 12 years of age should consult a doctor before use.*

* 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.