Lido Rx
Product Images NDC 35781-0300

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Lido Rx (NDC 35781-0300). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Gensco Laboratories, 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

Lidorx Label 10ml Rev 11 2018

Drug facts and instructions panel for Lido Rx Lidocaine Hydrochloride 3%, a topical anesthetic solution. Includes dosage and administration directions, adverse reactions, warnings, storage instructions, and lists active and inactive ingredients. Manufactured for Gensco Pharma, LLC in Miami, FL. The label advises applying a thin layer 3-4 times daily and cautions against use in certain populations.*

FDA Label Image

Lidorx Label 30ml Rev 11 2018

This Drug Facts panel for Lido Rx topical anesthetic with Lidocaine HCl 3% details dosage and administration instructions, potential adverse reactions, and warnings including use restrictions and methemoglobinemia precautions. It lists the active ingredient Lidocaine Hydrochloride 3% and inactive ingredients. Storage instructions and manufacturer contact information for Gensco Pharma, LLC are also provided.*

FDA Label Image

Lidorx Label 90ml Rev 11 2018

Drug Facts panel for Lido Rx Lidocaine HCl 3% topical anesthetic. It includes dosage instructions to apply a thin layer 3-4 times daily, warnings about potential adverse reactions and use precautions, storage conditions, and lists active and inactive ingredients. The label notes the net contents as 3.04 fl oz (90ml) and provides manufacturer information for Gensco Pharma, LLC.*

* 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.