Lidocaine Pain Relief Gel-patch
Product Images NDC 83602-158

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Lidocaine Pain Relief Gel-patch (NDC 83602-158). 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

Label_bag (Label Bag)

The packaging for Sumifun LIDOCAINE PAIN RELIEF Gel-Patch features a predominantly black background with white and gold text. It displays the product name with 4% lidocaine strength prominently and indicates it is a topical patch for numbing muscle and relieving pain. The front shows an outline of a human body highlighting common patch application areas including knee, back, neck, elbow, and shoulders. The back panel includes detailed drug facts, active and inactive ingredients, warnings, directions for use, and illustrated step-by-step usage instructions. The labeler is Guangzhou Liuquanmiao Import & Export Trade Co., Ltd.*

FDA Label Image

Label_box (Label Box)

Packaging label for LIDOCAINE PAIN RELIEF Gel-Patch containing 4% lidocaine in topical patch form. The label highlights pain relief for muscles and joints including knee, back, neck, elbow, and shoulder. The package size is 18 patches, each measuring 5.5" x 3.94" (14 cm x 10 cm). Labeler is Guangzhou Liuquanmiao Import & Export Trade Co., Ltd. The label includes drug facts, directions for use, warnings, inactive ingredients, and manufacturer contact information.*

FDA Label Image

Usage (Usage)

Instructional diagram showing usage steps for Lidocaine Pain Relief Gel-Patch topical patch. Four numbered illustrations depict removing the patch from outer packaging, partially peeling back protective film, placing the patch on the affected area, and removing remaining film while pressing the patch to skin.*

* 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.