Lidocaine Hydrochloride Injection, Solution
Product Images NDC 0404-9797

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Lidocaine Hydrochloride (NDC 0404-9797). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Henry Schein, Inc., 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

Formula1.jpg (Formula1)

Chemical structure of lidocaine hydrochloride showing a benzene ring with two methyl groups, an amide linkage, and a tertiary amine bonded to two ethyl groups, with HCl indicated as part of the structure.*

FDA Label Image

Image1.jpg (Image1)

A data table listing drug classes and examples. Classes include Nitrates/Nitrites, Local anesthetics, Antineoplastic agents, Antibiotics, Antimalarials, Anticonvulsants, and Other drugs, with examples such as lidocaine under Local anesthetics and nitric oxide under Nitrates/Nitrites.*

FDA Label Image

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A table listing various procedures for Lidocaine Hydrochloride Injection (without epinephrine), showing concentration percentages, volume in mL, and total dose in mg for each procedure. Procedures include infiltration, peripheral nerve blocks, dental, intercostal, paravertebral, pudendal, paracervical, obstetrical analgesia, and sympathetic nerve blocks with corresponding dosage parameters.*

FDA Label Image

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Label for Lidocaine Hydrochloride 2% Injection, USP, with a concentration of 20 mg/mL in a 50 mL multiple-dose vial. The label indicates use for infiltration and nerve block, with storage instructions and warnings. It is packaged by Henry Schein, Inc., located in Bastian, VA, with an NDC of 0404-9797-50.*

* 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.