Mepivacaine Injection, Solution
Product Images NDC 66975-406

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Mepivacaine (NDC 66975-406). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Benco Dental, 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

66975 406 51 Gtin

Packaging label for Mepivacaine HCl 3% (30 mg/mL) Injection without Vasoconstrictor, a submucosal injection solution. The label indicates it is distributed by Benco Dental and manufactured by Navel Pharmaceutical of Canada. The product is presented in 50 single-dose cartridges of 1.7 mL each, intended for dental block and infiltration. The label features the Graham Chemical Co. logo and includes barcodes and regulatory text.*

FDA Label Image

Chemical Structure 1 (Mepivacaine 01)

Chemical structure of mepivacaine hydrochloride showing its molecular formula C15H22N2·HCl and molecular weight 282.81. The diagram includes the aromatic ring and the piperidine ring characteristic of the compound.*

FDA Label Image

Chemical Structure 2 (Mepivacaine 02)

Chemical structure of Mepivacaine Hydrochloride showing the molecular formula C9H13NO3 and molecular weight 183.21. The structure includes a benzene ring with two hydroxyl groups and a side chain containing hydroxyl and amino groups.*

FDA Label Image

Symbol (Mepivacaine 03)

Mepivacaine 30 mg/mL injection solution in a clear vial with a white and green label. The label shows the product name, concentration, and route as submucosal injection. The vial is sealed with a gray rubber stopper and aluminum cap. The labeler is Benco Dental.*

* 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.