Lidocaine Hydrochloride Injection, Solution
Product Images NDC 0404-9763

Product Visual Gallery

This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Lidocaine Hydrochloride (NDC 0404-9763). 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

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Chemical structure of lidocaine hydrochloride showing the molecular arrangement of its components, including aromatic ring with methyl groups, amide linkage, and diethylamine group attached to a hydrochloride.*

FDA Label Image

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A data table presenting drug classes in one column and corresponding examples of drugs in the other. Included classes are Nitrates/Nitrites, Local anesthetics, Antineoplastic agents, Antibiotics, Antimalarials, Anticonvulsants, and Other drugs with several example drugs listed for each.*

FDA Label Image

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A table presenting dosing parameters for Lidocaine Hydrochloride Injection (without epinephrine) for various medical procedures. It lists procedure types, concentration percentages (0.5 to 2%), volume ranges in milliliters (1 to 60 mL), and corresponding total dose ranges in milligrams (5 to 300 mg), covering infiltration, peripheral nerve blocks, obstetrical analgesia, and sympathetic nerve blocks.*

FDA Label Image

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FDA Label Image

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Label for Lidocaine HCl 1% injection solution, 10 mg/mL strength in a 20 mL multiple-dose vial. The label shows usage instructions for infiltration and nerve block, cautions about storage and sterility, and includes manufacturer Henry Schein, Inc. with address. The label contains NDC barcode, lot and expiration placeholders, and regulatory information indicating prescription use only.*

* 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.