Lidodose
Product Images NDC 35781-0301

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Lidodose (NDC 35781-0301). 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

Carton

Lidodose Lidocaine Hydrochloride 3% topical anesthetic in a 1.0 mL single-use applicator. The green and white box features indications for use including preparation of skin for injection and pain relief for procedures such as dialysis and vaccinations. Labeler is Gensco Laboratories, LLC. The package is marked for professional use only and includes instructions, warnings, storage, and ingredient information.*

FDA Label Image

Insert

The image shows a multi-panel drug facts and usage instructions label for Lidodose Topical Anesthetic by Gensco Laboratories, LLC. It includes dosage and administration guidelines for adults, children, and infants, warnings about allergic reactions and proper use, a complete ingredient list with the active ingredient Lidocaine Hydrochloride (4%), and contact information for questions or comments. The label also details product purpose, uses, storage conditions, and inactive ingredients.*

FDA Label Image

Lidodose

Lidodose topical anesthetic containing Lidocaine Hydrochloride 3%, in a single-use 1.0 mL applicator for skin preparation before injections. The packaging highlights its use for pain relief in procedures like dialysis and vaccinations. Manufactured by Gensco Laboratories, 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.