Dr.johnes Liquid Skin Wart Corn Remover Solution
Product Images NDC 85818-004

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Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Dr.johnes Liquid Skin Wart Corn Remover (NDC 85818-004). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Dr.johnes 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.

Product Images & Figures Index

FDA Label Image

Package Of Dr. Johnes® Liquid Skin Wart Corn Remover 17% Salicylic Acid (Dr Johnes Wart Remover 1)

Package Of Dr. Johnes® Liquid Skin Wart Corn Remover 17% Salicylic Acid (Dr Johnes Wart Remover 1)
Packaging label for Dr.Johnes Liquid Skin Wart Corn Remover topical solution containing 17% Salicylic Acid. The dark blue carton highlights the product name, strength, and features such as a fast-acting film formula with botanical extracts and bee venom. The label includes drug facts, usage directions, warnings, inactive ingredients, and distributor information (Dr.Johnes LLC). The net quantity is 0.65 fl oz (20 mL).*
FDA Label Image

Package Of Dr. Johnes® Liquid Skin Wart Corn Remover 17% Salicylic Acid (Dr Johnes Wart Remover2)

Package Of Dr. Johnes® Liquid Skin Wart Corn Remover 17% Salicylic Acid (Dr Johnes Wart Remover2)
Dr.Johnes Liquid Skin Wart Corn Remover 17% Salicylic Acid topical solution label showing a 20 mL size. The label highlights max strength, fast-acting film formula, and targeted wart and corn care for hands and feet. Additional details mention infusion with bee venom and botanical extracts, and the product is for external use only, designed for precise application and removing rough skin buildup.*

* 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.