Auixudin Lidocaine Pain Relief Gel-patch
Product Images NDC 83559-019

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 Auixudin Lidocaine Pain Relief Gel-patch (NDC 83559-019). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Henan Enokon Medical Instrument 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

40patch (40patch)

40patch (40patch)
Auixudin Lidocaine Pain Relief Gel-Patch packaging label features a predominantly dark blue design with white and yellow text. The front highlights the product name, 4% lidocaine strength, and maximum strength pain relief gel-patch in a 5.5 x 3.94 inch patch size. It includes 40 patches and mentions use on knee, back, neck, elbow, and shoulders. The labeler, Henan Enokon Medical Instrument Co., Ltd, and directions for use are visible, along with a Drug Facts panel outlining active ingredient, warnings, and inactive ingredients. Illustrated application instructions and QR codes for a quick start guide are also present.*
FDA Label Image

5patch (5patch)

5patch (5patch)
Auixudin Lidocaine Pain Relief Gel-Patch 4% topical patch packaging label, containing 5 patches. The front display shows the product name, pain relief claims for minor aches, and highlights a flexible adhesive along with secure-hold overlay strips. The label includes directions, warnings, and ingredient information, along with a QR code for a quick start guide. Manufacturer is Henan Enokon Medical Instrument Co., Ltd.*

* 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.