Lidocaine Hydrochloride Injection, Solution
Product Images NDC 71872-7233

3 FDA label images from Medical Purchasing Solutions, Llc · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Lidocaine Hydrochloride (NDC 71872-7233). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Medical Purchasing Solutions, 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

71872-7223-1.pdp (71872 7233 1)

71872-7223-1.pdp (71872 7233 1)
Label for Lidocaine Hydrochloride Injection USP 2% (20 mg/mL) in a 20 mL multiple dose vial. The label includes drug concentration, volume, intended use for infiltration and nerve block, storage instructions, preservatives information, and distributor details for Medical Purchasing Solutions, LLC, Scottsdale, AZ. Manufacturer is listed as AruMedics Pharma, New Jersey.*
FDA Label Image

Package Label-principal Display Panel (2% 400 mg per 20 mL (20 mg / mL))

Package Label-principal Display Panel (2% 400 mg per 20 mL (20 mg / mL))
Label for Lidocaine HCl Injection, USP 2% solution, 400 mg per 20 mL (20 mg/mL), in a 20 mL multiple dose vial. The label states use for infiltration and nerve block, not for caudal or epidural use. Distributed by AuroMedics Pharma LLC and made in India. Includes storage instructions, preservative information, and barcode.*
FDA Label Image

Lidocaine Hydrochloride Chemical Structure (Lidocaine Str)

Lidocaine Hydrochloride Chemical Structure (Lidocaine Str)
Chemical structure diagram of Lidocaine Hydrochloride showing the molecular arrangement including aromatic ring, amide linkage, and diethylamino group.*

* 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.