Xylocaine Injection, Solution
Product Images NDC 0404-9977

Product Visual Gallery

This gallery contains 10 technical images submitted to the FDA as part of the official labeling for Xylocaine (NDC 0404-9977). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Henry Schein, 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

Formula1.jpg (Formula1)

Chemical structure diagram of the active ingredient Lidocaine Hydrochloride, showing its molecular arrangement with labeled functional groups and hydrochloride (HCl) component.*

FDA Label Image

Formula2.jpg (Formula2)

Chemical structure diagram showing the molecular arrangement of the active ingredient, Lidocaine Hydrochloride and Epinephrine, in Xylocaine injection solution.*

FDA Label Image

Image1.jpg (Image1)

A data table listing drug classes in one column and example drugs in another. Classes include Nitrates/Nitrites, Local anesthetics, Antineoplastic agents, Antibiotics, Antimalarials, Anticonvulsants, and Other drugs, with examples such as lidocaine under Local anesthetics and acetaminophen under Other drugs.*

FDA Label Image

Image2.jpg (Image2)

A data table showing dosing information for Xylocaine (lidocaine hydrochloride) injection without epinephrine. Columns include procedure type, concentration percentage, volume in mL, and total dose in mg. Procedures listed cover infiltration, peripheral nerve blocks, paracervical, sympathetic nerve blocks, central neural blocks, and caudal, with corresponding dosing ranges.*

FDA Label Image

Image3.jpg (Image3)

A data table listing Lidocaine Hydrochloride Injection, USP product codes, unit of sale, strengths, and packaging details. Strengths range from 0.5% to 2%, available in multiple dose vial sizes of 10 mL, 20 mL, and 50 mL, with respective National Drug Codes (NDCs) provided for each variant.*

FDA Label Image

Image4.jpg (Image4)

A data table listing various NDC codes for Xylocaine (lidocaine HCl injection, USP) in multiple strengths with packaging details. It shows product codes, unit of sale, strength (ranging from 0.5% to 2%), and packaging formats including single dose vials and plastic ampules in various volumes from 2 mL to 50 mL.*

FDA Label Image

Image5.jpg (Image5)

Tables listing NDC codes, units of sale, strengths, and package sizes for Xylocaine (lidocaine HCl and epinephrine injection, USP) with epinephrine concentrations of 1:100,000 and 1:200,000. Strengths range from 0.5% to 2% in various multiple dose vial sizes from 10 mL to 50 mL.*

FDA Label Image

Image6.jpg (Image6)

A data table listing various product codes, units of sale, strengths, and package sizes for Xylocaine-MPF (lidocaine HCl and epinephrine injection, USP) with epinephrine 1:200,000. The table details NDC codes for 1%, 1.5%, and 2% strengths available in 10 mL, 20 mL, and 30 mL single dose vials with varying pack sizes.*

FDA Label Image

Label1.jpg (Label1)

Label for Xylocaine 1% (Lidocaine HCl and Epinephrine 1:100,000) Injection, USP, 10 mg/mL, 20 mL multiple-dose vial. The label includes storage instructions, warnings, and manufacturer information for Henry Schein, Inc., located in Bastian, VA. It also displays the NDC 0404-9977-20 and barcode.*

FDA Label Image

Label2.jpg (Label2)

Label for Xylocaine 1% Injection, USP, containing Lidocaine HCl and Epinephrine 1:100,000 at 500 mg per 50 mL in a multiple dose vial. The label includes storage instructions, usage warnings, and manufacturer details, Henry Schein, Inc., located in Bastian, VA. The product is prescription only and for infiltration and nerve block usage.*

* 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.