Menthol Powder
Product Images NDC 82442-211

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Product Visual Gallery

This gallery contains 1 technical images submitted to the FDA as part of the official labeling for Menthol (NDC 82442-211). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Target 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

Carton (Target Upup Medicated Foot Powder 50 113tg 02 51 113tg 02)

Carton (Target Upup Medicated Foot Powder 50 113tg 02 51 113tg 02)
Drug Facts label for Menthol Maximum Strength Medicated Foot Powder Talc Free 10 mg/g topical powder by Target Corporation. The label lists menthol 1.0% as the active ingredient for external analgesic use, temporary relief of minor skin irritation pain and itching. Warnings include external use only and avoiding eye contact. Directions for use and inactive ingredients are also provided.*

* 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.