Lidocaine Hydrochloride And Epinephrine
Product Images NDC 61699-3182

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Lidocaine Hydrochloride And Epinephrine (NDC 61699-3182). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Us Medsource, Llc, 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

Label (Label 61699 3182 3)

Label for Lidocaine Hydrochloride 2% and Epinephrine 1:100,000 Injection, USP, 20 mg/mL strength in a 50 mL multiple dose glass vial. Packaged by US MedSource, LLC, Sarasota, FL. The label includes storage instructions, ingredient details, a barcode, and a small image of the vial with a red cap and red and white label. Marked as RX only.*

FDA Label Image

Structural Formula Lidocaine Hydrochloride Usp (Lidocaine Hydrochloride And Epinephrine Injection Usp2 Figure 1 Lidocaine Hydrochloride And Epinephrine Inj Usp Figure 1)

Chemical structure diagram of Lidocaine Hydrochloride showing its molecular composition, including methyl groups attached to a benzene ring, an amide linkage, a diethylamino group, a hydrochloride component, and a water molecule. The structure visually represents key atoms and bonds typical for lidocaine's chemical identity.*

FDA Label Image

Structrual Formula Epinephrine, Usp (Lidocaine Hydrochloride And Epinephrine Injection Usp2 Figure 2 Lidocaine Hydrochloride And Epinephrine Inj Usp Figure 2)

Chemical structure of the active ingredient depicted in the image, showing a phenol ring with two hydroxyl groups, a hydroxyl group attached to a carbon, and an adjacent methylamine side chain.*

* 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.