Lidocaine Hydrochloride Injection, Solution
Product Images NDC 71872-7144

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 71872-7144). 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.

Product Images & Figures Index

FDA Label Image

Pdp (7144)

Pdp (7144)
Label for Lidocaine Hydrochloride Injection, USP 2% (20 mg/mL) single dose vial, 100 mg/5 mL, by Medical Purchasing Solutions, LLC. It indicates usage for infiltration and nerve block, including caudal and epidural use. The label notes the vial stopper is latex-free, lists inactive ingredients, dosage advice, storage conditions, and manufacturer details.*
FDA Label Image

Package Label-principal Display Panel (2% 100 mg/5 mL (20 mg/mL))

Package Label-principal Display Panel (2% 100 mg/5 mL (20 mg/mL))
Label for Lidocaine Hydrochloride Injection USP 20 mg/mL (2%) solution in a 5 mL single-dose vial. The label specifies use for infiltration and nerve block including caudal and epidural use. It is preservative-free, sterile, nonpyrogenic, with instructions for storage and handling. Manufactured for AuroMedics Pharma LLC by a facility in India.*
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, and tertiary amine groups with associated hydrochloride (HCl).*

* 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.