Lidocaine Hydrochloride Injection, Solution
Product Images NDC 71872-7184

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Lidocaine Hydrochloride (NDC 71872-7184). 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

71872-7184-1.pdp (71872 7184 1)

This is a description of a drug product called "1% Lidocaine HCI Injection, USP". It comes in a 200mg/20mL (10 mg/mL) multiple-dose flip-top vial and is used for infiltration and nerve block. The product is not recommended for epidural and caudal use. It contains lidocaine hydrochloride, sodium chloride, and methylparaben as a preservative. The vial is sterile and nonpyrogenic. The usual dose should be determined via the insert. The product should be stored at 20° to 25°C (68 to 77°F) and manufactured by Hospira Inc. The product is also repackaged and distributed by Medical Purchasing Solutions.*

FDA Label Image

Chemical Structure (Lidocaine 01)

FDA Label Image

Hospira Logo (Lidocaine 02)

FDA Label Image

Principal Display Panel (200 mg/20 mL Vial Label)

This is a description of Lidocaine HCI Injection, a sterile solution used for infiltration and nerve block. It contains 200 mg/20 mL (10 mg/mL) of Lidocaine hydrochloride along with sodium chloride (7mg) and methylparaben (1mg) as preservatives. It is not recommended for epidural and caudal use. The pH is adjusted with HCl and/or NaOH and it must be stored at 20 to 25°C (68 to 77°F). The usual dosage can be found in the insert. This solution is distributed by Hospira, Inc.*

* 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.