Menthol Pain Relief Gel-roll On Gel
Product Images NDC 83602-333

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Menthol Pain Relief Gel-roll On (NDC 83602-333). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Guangzhou Liuquanmiao Import & Export Trade Co., Ltd., 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

Container Label (333 0)

Container Label (333 0)
Label for Menthol Pain Relief Gel-Roll On, containing 4% Menthol in a 2.5 FL OZ (74 ml) gel dosage form. The product is marketed under the brand name Sumifun. It highlights features such as fast acting, instant deep cooling sensation, and fast absorbing for rapid relief. The label includes detailed drug facts, usage instructions, warnings, directions, and a list of inactive ingredients. The labeler is Guangzhou Liuquanmiao Import & Export Trade Co., Ltd.*
FDA Label Image

Package Label (333 1)

Package Label (333 1)
Packaging label for Menthol Pain Relief Gel-Roll On by Guangzhou Liuquanmiao Import & Export Trade Co., Ltd. The label features 4% menthol in a 2.5 FL OZ (74 ml) gel formulation. The product branding includes Sumifun and highlights fast acting, instant deep cooling sensation, and rapid absorption for relief. The label also shows illustrations indicating use on knee, foot, elbow, back, and neck. Included is a Drug Facts panel detailing active ingredients, uses, warnings, directions, and inactive ingredients.*

* 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.