Gold Bond Medicated Maximum Strength Foot
Product Images NDC 41167-0171

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Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Gold Bond Medicated Maximum Strength Foot (NDC 41167-0171). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Chattem, 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.

Product Images & Figures Index

FDA Label Image

Principal Display Paneltalc-freegold Bondmaximum Strengthfoot Powdernet Wt 10 Oz (283 G) (Gold Bond Medicated Maximum Strength Foot Powder 01)

Principal Display Paneltalc-freegold Bondmaximum Strengthfoot Powdernet Wt 10 Oz (283 G) (Gold Bond Medicated Maximum Strength Foot Powder 01)
Label of Gold Bond Medicated Maximum Strength Foot powder by Chattem, Inc. The label indicates the product is talc-free, medicated, and contains menthol 1%. It features claims of a unique triple action formula that absorbs moisture, controls odor, and relieves itch. The net weight is 10 ounces (283 grams).*
FDA Label Image

Principal Display Paneltalc-freegold Bondmaximum Strengthfoot Powdernet Wt 10 Oz (283 G) (Gold Bond Medicated Maximum Strength Foot Powder 02)

Principal Display Paneltalc-freegold Bondmaximum Strengthfoot Powdernet Wt 10 Oz (283 G) (Gold Bond Medicated Maximum Strength Foot Powder 02)
Drug Facts panel for Gold Bond Medicated Maximum Strength Foot Powder by Chattem, Inc. Lists menthol 1% as the active anti-itch ingredient and details uses for temporary relief of pain and itch from minor skin irritations on the foot. Includes warnings, directions for adults and children, and inactive ingredients such as corn starch and peppermint oil. Also provides storage and safety instructions.*

* 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.