Lidocaine Injection, Solution
Product Images NDC 0362-0898

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Lidocaine (NDC 0362-0898). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Septodont, 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

Composition Table (Composition)

A composition table for Lidocaine Hydrochloride and Epinephrine Injection, USP, showing brand names, concentrations and dilutions of lidocaine hydrochloride and epinephrine, and formulas per single dose cartridge including sodium chloride, potassium metabisulfite, and edetate disodium amounts. It includes two product variants with different epinephrine dilutions (1:50,000 and 1:100,000).*

FDA Label Image

Principal Display Panel (1.7 mL Cartridge Carton)

Label for Lidocaine HCl 2% and Epinephrine 1:100,000 Injection by Septodont, Inc., for dental use. The box specifies submucosal injection, dental block, and infiltration only. Contains 50 cartridges of 1.7 mL each. Manufactured by Novocol Pharmaceutical of Canada Inc. The label includes dosage component details and cautions about color and precipitate in the solution.*

FDA Label Image

Chemical Structure (Lidocaine 01)

Chemical structure of lidocaine hydrochloride. The diagram shows the molecular arrangement of lidocaine with two methyl groups attached to a benzene ring and diethyl amine substituents, along with the hydrochloride component.*

FDA Label Image

Chemical Structure (Lidocaine 02)

Chemical structure of Lidocaine showing its molecular arrangement with a benzene ring, hydroxyl groups, and amide linkage.*

* 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.