Antifungal Liquid
Product Images NDC 82442-998

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This gallery contains 1 technical images submitted to the FDA as part of the official labeling for Antifungal Liquid (NDC 82442-998). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Target Corporation, 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 (Target Upup Antifungal Liquid Solution 53 218tg)

Carton (Target Upup Antifungal Liquid Solution 53 218tg)
This is a description of a Maximum Strength Antifungal Liquid containing Tolnaftate 1%. The product is designed to treat fungal infections on cuticles, around nail edges, and skin under nail tips. It is clinically effective in treating athlete’s foot and ringworm, with the ability to prevent reoccurrence with daily use. The liquid is meant for external use only and should be avoided near the eyes. The product must not be used on children under 2 years of age without doctor's instructions. In case of irritation or no improvement after 4 weeks, users are advised to seek medical help. The liquid is not effective on the scalp or nails. The directions for use include washing and drying feet, wearing well-fitting shoes, and applying the product daily for 4 weeks. If the condition persists, consulting a doctor is recommended. This antifungal liquid is not effective on the scalp or nails. It contains active ingredient Tolnaftate 1% and other inactive ingredients. The product is distributed by Target Corporation and should be kept away from freezing temperatures.*

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