Menthol Pain Relief Gel-patch
Product Images NDC 83602-132

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-patch (NDC 83602-132). 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.

Product Images & Figures Index

FDA Label Image

01 (132 01)

01 (132 01)
Menthol Pain Relief Gel-Patch packaging label in 5% strength, containing 1 patch measuring 3.93 x 5.51 inches (10 x 14 cm). The label highlights fast-acting, long-lasting (8-hour), and targeted relief for sore muscles, backaches, stiff neck, and joint pain. Labeled by Guangzhou Liuquanmiao Import & Export Trade Co., Ltd., it includes usage direction icons for knee, back, neck, elbow, and shoulder. Drug facts panel details topical analgesic purpose, warnings, directions, and inactive ingredients.*
FDA Label Image

15 (132 15)

15 (132 15)
Menthol Pain Relief Gel-Patch 5% menthol topical patch packaging label featuring the brand Sumifun. The label indicates 15 patches sized 3.93 x 5.51 inches. It highlights fast acting, powerful targeted relief, and long-lasting effects up to 8 hours. Usage instructions with illustrations show removing the outer package, peeling back the protective film, placing the patch on affected area, and removing remaining film. The label also includes a Drug Facts section, warnings, directions, inactive ingredients, and contact information for Guangzhou Liuquanmiao Import & Export Trade Co., Ltd. The label is predominantly blue and yellow with white text accents.*

* 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.