Profoot Pain Relief Patches Kit
Product Images NDC 29784-600

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Profoot Pain Relief Patches (NDC 29784-600). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Rooftop Consumer Health, 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

Carton (Carton)

Profoot Pain Relief Patches kit packaging label contains 6 patches in two shapes for feet and heels. The label highlights temporary relief from foot and heel pain, sprains, strains, and bruises, featuring active ingredients camphor, menthol, and methyl salicylate. The labeler is Rooftop Consumer Health, Inc.*

FDA Label Image

Image Description (Label1)

Profoot Pain Relief Patches kit contains 1 patch with HeelFit shape, designed to fit heels, measuring 5 x 3 inches. The label lists active ingredients Camphor 1.2%, Menthol 5.7%, and Methyl Salicylate 6.4%. It is distributed by Rooftop Consumer Health, Inc. The packaging highlights temporary relief from foot and heel pain, sprains, strains, and bruises.*

FDA Label Image

Image Description (Label3)

Drug Facts panels for Profoot Pain Relief Patches with active ingredients camphor 1.2%, menthol 5.7%, and methyl salicylate 6.3%, listed as topical analgesics. The panels provide uses for temporary relief of minor muscle and joint pain, various warnings, directions for use, inactive ingredients, and contact information for the manufacturer, Rooftop Consumer Health, Inc.*

* 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.