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.

Product Images & Figures Index

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.*
FDA Label Image

Lidovial (Lidovial)

Lidovial (Lidovial)
Label for Lidocaine HCl Injection, USP 2% (20 mg/mL), 20 mL multiple dose vial by AuroMedics Pharma LLC. The label indicates 400 mg per 20 mL, intended for infiltration and nerve block, with specific storage instructions and warnings against use in caudal or epidural applications. Distributed by AuroMedics Pharma LLC, made in India.*
FDA Label Image

Lidolabel (Lidolabel)

Lidolabel (Lidolabel)
Label for Lidocaine Hydrochloride 20 mg/mL injection solution, USP, in a 20 mL multiple-dose vial. The product is indicated for infiltration and nerve block, containing 400 mg per 20 mL vial. Label shows lot number, expiration date, preservative methylparaben, and storage instructions at 20° to 25°C. Distributed by AuroMedics Pharma and repackaged by Medical Purchasing Solutions, LLC, Scottsdale, AZ.*

* 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.