Dermatool Fungal Nail Treatment Liquid
Product Images NDC 72839-510

Product Visual Gallery

This gallery contains 1 technical images submitted to the FDA as part of the official labeling for Dermatool Fungal Nail Treatment (NDC 72839-510). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Derma Care Research Labs, 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

Carton (Sidny Reversetuckbox 09.03.23 (1) (1) Copy)

Drug Facts and product labeling for Dermatool Fungal Nail Treatment topical liquid, 0.5 fl oz (15 mL) containing 1% Tolnaftate active ingredient. The panel includes uses, warnings, directions for use, other storage information, inactive ingredients, and product features such as antifungal action, applicability to toes and fingers, and free of parabens, propylene glycol, and sulfates. Contact and distributor details for Dermatool are also shown.*

* 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.