Lidocan Iv Patch
Product Images NDC 59088-910

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Lidocan Iv (NDC 59088-910). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Puretek Corporation, 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

Drug (Drug Asso)

A table categorizing drug examples by pharmacologic class. Classes include Nitrates/Nitrites with agents such as nitric oxide and nitroglycerin; Local anesthetics including lidocaine and bupivacaine; Antineoplastic agents like cyclophosphamide and hydroxyurea; Antibiotics such as dapsone and sulfonamides; Antimalarials including chloroquine; Anticonvulsants like phenobarbital and valproate; and a category for Other drugs including acetaminophen and metoclopramide.*

FDA Label Image

Label (Label)

Lidocan IV Lidocaine Patch 5% packaging label showing each patch contains 700 mg lidocaine in an aqueous base. The label includes inactive ingredients, usage instructions, storage conditions, and a warning to keep patches away from children and pets. The patch size is 10 cm by 14 cm. The labeler is PureTek Corporation.*

FDA Label Image

Graphs (Graphs)

A line graph depicting plasma lidocaine concentration (ng/mL) over time in hours up to 72 hours. The graph shows repeated peaks and troughs in plasma lidocaine levels approximately every 24 hours, illustrating a periodic pattern in plasma concentration.*

FDA Label Image

Molecule (Molecule)

Chemical structure of lidocaine showing its aromatic ring, amide bond, and diethylamino side chain as depicted in the diagram.*

* 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.