Lidocaine Injection, Solution
Product Images NDC 51004-2105

View Photos of 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 (NDC 51004-2105). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Novocol Pharmaceutical Of Canada, 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

Principal Display Panel-1.7 mL Cartridge Carton (2764 1 L100 Atlanta Dental Us Pc Gtin)

Principal Display Panel-1.7 mL Cartridge Carton (2764 1 L100 Atlanta Dental Us Pc Gtin)
Packaging label for Lidocaine HCl 2% injection solution, submucosal, containing 34 mg/1.7 mL (20 mg/mL) of Lidocaine Hydrochloride and Epinephrine Bitartrate. The label indicates single-dose cartridges of 1.7 mL each, for dental block and infiltration anesthesia. Manufactured by Novocol Pharmaceutical of Canada, Inc., and labeled by Advance Dental Products.*
FDA Label Image

Epinephrine (Epinephrine)

Epinephrine (Epinephrine)
Chemical structure diagram showing the molecular arrangement of the active ingredient in the product, Lidocaine Hydrochloride and Epinephrine Bitartrate. The structure includes a benzene ring with hydroxyl groups and a side chain featuring nitrogen and carbon atoms.*
FDA Label Image

Lidocaine Hydrochloride (Lidocaine Hydrochloride)

Lidocaine Hydrochloride (Lidocaine Hydrochloride)
Chemical structure diagram of Lidocaine Hydrochloride, showing the molecular arrangement of atoms including aromatic ring with methyl groups, amide linkage, and diethylamino side chains bonded to hydrochloride.*

* 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.