Liquid Callus Remover Liquid
Product Images NDC 56104-501

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Liquid Callus Remover (NDC 56104-501). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Premier Brands Of America Inc., 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

Image 2 (Endzone Lccr 50 030ez)

Label for Endzone Liquid Callus Remover, a medicated topical liquid containing 17% salicylic acid, used for removing corns and calluses. The label includes warnings such as keeping away from fire, avoiding use on infected skin, and instructions to close cap tightly after use. The container size is 0.33 fl. oz. (9.8 mL). Distributed by Premier Brands of America Inc.*

FDA Label Image

Image 1 (Endzone Lccr High Rise 53 030ez)

Packaging label for EndZone Liquid Callus Remover contains 0.33 fl oz (9.8 mL) of topical liquid with 17% salicylic acid as the active ingredient. The label design features navy blue and orange colors, includes application warnings, directions, ingredients, and storage instructions, and states it is a medicated product by Premier Brands of America Inc. for safe removal of corns and calluses.*

* 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.