Dermatool Fungal Nail Treatment Liquid
Product Images NDC 72839-510

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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.

Product Images & Figures Index

FDA Label Image

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

Carton (Sidny Reversetuckbox 09.03.23 (1) (1) Copy)
This is a drug information label that contains details about the active ingredient, usage, warning, directions, and other information. The active ingredient is Tolnaftate and is used as an antifungal treatment for athlete's foot, tinea pecs, tinea corpori, and ringworm. It helps to relieve itching, scaling, cracking, redness, and soreness. The label provides instructions on how to use the product and warns not to use it on children under 2 years old unless directed by a doctor. It suggests consulting a doctor in case of irritation or no improvement within 4 weeks. Besides, the inactive ingredients and the product's size are also given. The label also describes Dermatool as a fast-acting, medicated formula that contributes to nail recovery. Contact information of the manufacturer is also provided.*

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