North Woods Derma Foam E-2 Soap
Product Images NDC 53125-817

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Product Visual Gallery

This gallery contains 1 technical images submitted to the FDA as part of the official labeling for North Woods Derma Foam E-2 (NDC 53125-817). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Superior Chemical 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

71729-00 Superior Derma Foam (71729 00 Superior Derma Foam E2)

71729-00 Superior Derma Foam (71729 00 Superior Derma Foam E2)
This is a drug facts label for a hand wash product containing 0.13% Benzalkonium Chloride as an active ingredient to decrease bacteria on the skin. It provides directions for use and warning statements for external use only and to avoid eye contact. It also instructs to seek medical help if irritation or redness develops or if the condition persists for more than 72 hours. The product is recommended for repeated use and includes inactive ingredients such as water, coco-glucoside, laurtrimonium chioride, cocamidopropylamine oxide, and allantoin. It comes in a 1L container and is made in the USA. Contact information is provided for questions or comments.*

* 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.