Lidopro Patch
Product Images NDC 80425-0582

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Product Visual Gallery

This gallery contains 1 technical images submitted to the FDA as part of the official labeling for Lidopro (NDC 80425-0582). 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 Patch #30 (Lidopro Patch 30 80425 0582 01)

Lidopro Patch #30 (Lidopro Patch 30 80425 0582 01)
Label for LidoPro Patch #30, a transdermal patch containing lidocaine and menthol. It includes package identifiers such as NDC 80425-0582-01, source NDC 83881-0403-30, and lot number 30LIP41230 with an expiration date of 2/28/2030. The label indicates storage at 20°-25°C and is packed by Advanced Rx of Tennessee, LLC, Nashville, TN.*

* 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.