Gold Bond Medicated Maximum Strength Foot Powder
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.

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)
This product is talc-free and offers maximum strength.*
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)
GOLD BOND Foot Powder Maximum Strength temporarily relieves the pain and itch associated with minor skin inflammations on the foot. It contains Menthol 1% as the active ingredient. It is for external use only and should not be used on the eyes. If the condition worsens, persists for more than 7 days or occurs again after a few days, consult a doctor. It should be kept out of reach of children and if swallowed, get immediate medical help. It contains inactive ingredients such as starch, sodium bicarbonate, acacia senega qun, and others. This product is manufactured by Sanofi.*

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