Lidocaine Hydrochloride And Epinephrine Injection, Solution
Product Images NDC 0404-9891

9 FDA label images from Henry Schein, Inc. · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 9 technical images submitted to the FDA as part of the official labeling for Lidocaine Hydrochloride And Epinephrine (NDC 0404-9891). 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

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Formula1.jpg (Formula1)
Chemical structure diagram showing the molecular formula of Lidocaine Hydrochloride, including its chemical groups and composition as hydrochloride and hydrate form.*
FDA Label Image

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Formula2.jpg (Formula2)
Chemical structure diagram of the active ingredient Lidocaine Hydrochloride and Epinephrine, showing its molecular arrangement with phenol groups, hydroxyl groups, and amine substitutions.*
FDA Label Image

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Image1.jpg (Image1)
A data table listing concentrations of Lidocaine Hydrochloride and Epinephrine along with corresponding levels of Lidocaine HCl (anhydrous), Epinephrine, and Sodium Chloride in mg/mL or mcg/mL. The table shows various dilution ratios and their associated component strengths.*
FDA Label Image

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This text panel provides information about specific available products of Lidocaine Hydrochloride and Epinephrine Injection, USP, recommended by Hospira for epidural anesthesia. It lists various concentrations and corresponding single-dose vial sizes, including 1% and 1.5% solutions with epinephrine 1:200,000 in 30 mL vials, and 2% solution with epinephrine 1:200,000 in 20 mL vials, as well as 1.5% with epinephrine 1:200,000 in 5 mL single-dose ampuls.*
FDA Label Image

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A table titled "Recommended Dosages Lidocaine Hydrochloride Injection, USP (without Epinephrine)" listing concentrations, volume in mL, and total dose in mg for various procedures. It includes infiltration, peripheral nerve blocks, sympathetic nerve blocks, and central neural blocks, with specific dose ranges for each procedure and notes that doses are guidelines and maximum dose should not be exceeded.*
FDA Label Image

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Table titled "Recommended Dosages" presenting dose concentration, volume, and total dose for Lidocaine Hydrochloride Injection USP (without Epinephrine). It outlines recommended dosages by procedure type including infiltration, peripheral nerve blocks, sympathetic nerve blocks, and central neural blocks, with specific values for concentration percentage, volume in milliliters, and total dose in milligrams.*
FDA Label Image

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Label1.jpg (Label1)
Label of Lidocaine Hydrochloride 1% and Epinephrine 1:100,000 Injection, USP, 30 mL multiple-dose vial. The label includes storage instructions, warnings against autoclaving, and advises to avoid use if discoloration or precipitate is present. It is packaged by Henry Schein, Inc., located in Bastian, VA, with an NDC of 0404-9891-20.*
FDA Label Image

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Label2.jpg (Label2)
Label for Lidocaine Hydrochloride 1% and Epinephrine 1:100,000 injection, US Pharmacopeia (USP) Multiple Dose, 20 mL vial. The label includes storage instructions to protect from light, avoid autoclaving, and keep at controlled room temperature. It states the product is for infiltration and nerve block only, not for epidural or caudal use. Packaged by Henry Schein, Inc., Bastian, VA, with an NDC barcode visible.*
FDA Label Image

Label3.jpg (Label3)

Label3.jpg (Label3)
Label for Lidocaine Hydrochloride and Epinephrine injection, USP multiple dose solution. The label shows concentrations of Lidocaine HCL 1% and Epinephrine 1:100,000 in a 50 mL vial. It includes storage instructions, warnings against epidural or caudal use, and packaging information by Henry Schein, Inc. with the NDC 0404-9891-50.*

* 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.