Qkit Procedure Tray
Product Images NDC 59365-9074

7 FDA label images from Coopersurgical, Inc. · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 7 technical images submitted to the FDA as part of the official labeling for Qkit Procedure Tray (NDC 59365-9074). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Coopersurgical, 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

The Structural Formula Of Lidocaine HCl. (Qkit 01)

The Structural Formula Of Lidocaine HCl. (Qkit 01)
Chemical structure diagram showing the molecular formula of the active ingredient, depicted as a compound with a benzene ring substituted with two methyl groups, an amide linkage, and diethylamino group, associated with hydrochloride (HCl).*
FDA Label Image

The Structural Formula Of Epinephrine. (Qkit 02)

The Structural Formula Of Epinephrine. (Qkit 02)
Chemical structure diagram showing a molecular formula with a benzene ring substituted with three hydroxyl groups (tri-hydroxybenzene) and a side chain containing a hydroxyl group, a methylated amine group, and a carbon chain. The diagram corresponds to a molecule related to the product data provided.*
FDA Label Image

How Supplied (Qkit 03)

How Supplied (Qkit 03)
A table showing various Xylocaine (lidocaine HCl) products differentiated by concentration, presence of epinephrine dilution, and packaging type including plastic ampules, single dose vials, and multiple dose vials with their corresponding volume in milliliters.*
FDA Label Image

Qkit Procedure Trayndc # 59365-9074-1 (Qkit 04)

Qkit Procedure Trayndc # 59365-9074-1 (Qkit 04)
QKit Procedure Tray for Loop Electrosurgical Excision Procedure by CooperSurgical, Inc. The label includes instructions for use, a detailed list of included components such as lidocaine with epinephrine, various surgical tools, and cautions. The label also contains product reference number 909074, manufacturer contact information, and spaces for lot number and expiration date.*
FDA Label Image

Principal Display Panelxylocaine (lidocaine HCl With Epinephrine)ndc 63323-482-17 (Qkit 05)

Principal Display Panelxylocaine (lidocaine HCl With Epinephrine)ndc 63323-482-17 (Qkit 05)
QKit Procedure Tray is not depicted in the image. The image shows a medication label for Xylocaine (lidocaine HCl and epinephrine injection, USP) 1% with epinephrine 1:100,000, 10 mL vial, multiple dose. The label includes usage instructions, storage conditions, and manufacturer information for Fresenius Kabi USA, LLC.*
FDA Label Image

Principal Display Panel8gm Ndc 59365-5006-0ferric Subsulfateaqueous (Qkit 06)

Principal Display Panel8gm Ndc 59365-5006-0ferric Subsulfateaqueous (Qkit 06)
Label for Wallach Ferric Subsulfate aqueous solution, indicating a concentration of 259 mg/g ferric subsulfate and an 8 gram quantity. The label includes storage instructions, a caution about prescription dispensing, and manufacturer information for Wallach Surgical Devices in Trumbull, Connecticut.*
FDA Label Image

Principal Display Panel8ml Ndc 59365-6064-0lugol’s (strong Iodine Solutions Usp) (Qkit 07)

Principal Display Panel8ml       Ndc 59365-6064-0lugol’s (strong Iodine Solutions Usp) (Qkit 07)
Label of Lugol's Strong Iodine Solution USP, 8 mL, showing active ingredients iodine 0.05 mg and potassium iodide 0.100 mg per mL. The label includes usage instructions for single use, storage conditions, manufacturer CooperSurgical, Inc., Trumbull, CT, and product NDC 59365-6064-0. The label also states the federal law caution against dispensing without prescription.*

* 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.