Lidopro Pain Relief Ointment
Product Images NDC 80425-0452

Product Visual Gallery

This gallery contains 1 technical images submitted to the FDA as part of the official labeling for Lidopro Pain Relief (NDC 80425-0452). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Advanced Rx Of Tennessee, Llc, 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

Lidopro Ointment (Lidopro Ointment 80425 0452 01)

Label for LidoPro Pain Relief ointment, containing Capsaicin and Lidocaine, in a 99 gram transdermal ointment form. The label includes the NDC number 80425-0452-01, lot information, expiration date 4/30/2026, and storage instructions (20°-25°C). It is marked for prescription use (Rx only) and labeled by Advanced Rx of Tennessee, LLC, Nashville, TN. The label also features a barcode and clinic pharmacy serial number.*

* 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.