Antifungal Liquid Maximum Strength Liquid
Product Images NDC 0363-7998

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Antifungal Liquid Maximum Strength (NDC 0363-7998). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Walgreens Company, 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

Label (Walgreens Anti Fungal Nail Liquid 50 121wg 02)

Label (Walgreens Anti Fungal Nail Liquid 50 121wg 02)
Label for Walgreens Antifungal Liquid Maximum Strength topical solution containing Tolnaftate 1% at 10 mg/mL. The product is a 1 fl. oz. (30 mL) liquid for antifungal treatment of fungus on fingers, toes, and skin around nails, marketed by Walgreens Company. The label includes usage warnings and ingredient information.*
FDA Label Image

Unit Carton (Walgreens Anti Fungal Nail Liquid 53 121wg 02)

Unit Carton (Walgreens Anti Fungal Nail Liquid 53 121wg 02)
Walgreens Antifungal Liquid Maximum Strength topical liquid containing Tolnaftate 1% is shown in its unfolded carton label. The label features white text on a dark blue background, highlighting the active ingredient and antifungal uses. The front displays a photo of the 1 fl. oz. (30 mL) amber glass bottle with white child-resistant cap and applicator brush. The label states it is a medicated antifungal for fungal infections on nails and skin. Warnings, drug facts, directions, and manufacturer details are printed on the carton.*

* 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.