Lidocaine Hci
Product Images NDC 51662-1230

Product Visual Gallery

This gallery contains 10 technical images submitted to the FDA as part of the official labeling for Lidocaine Hci (NDC 51662-1230). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Hf Acquisition Co. Llc, Dba Health First, 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

Syringe Carton (5 mL Syringe Box)

LIDOCAINE HCl 1% injection, USP, 50 mg/5 mL in a 5 mL glass ABBOTT ABBJOJECT unit of use syringe with a male luer lock adapter and 20-gauge protected needle. The label includes handling instructions, aseptic technique warnings, and dosage form information. It is labeled for intravenous use for cardiac arrhythmias and marked for prescription only. Manufactured by Hospira and labeled by HF Acquisition Co. LLC, DBA Health First.*

FDA Label Image

Serialized Label (51662 1230 1 Lidocaine 5ml Serialized Label On Box)

Box label of LIDOCAINE HCl 1% Injection, USP with a concentration of 50 mg per 5 mL. The product is distributed by HF Acquisition Co., LLC, Mukilteo, WA. The label includes storage instructions, dosage reference, and safety information about needle use and disposal.*

FDA Label Image

51662 1230 2 Pouch Labeling

Label for LIDOCAINE HCl Injection, USP 1% 50 mg/5 mL (10 mg/mL) in a 5 mL syringe. The label includes NDC 51662-1230-2, lot number 123456, and expiration date 2030-01-01. It specifies the medication is for intravenous use with detailed composition and storage instructions. Manufactured by HF Acquisition Co., LLC, Mukilteo, WA.*

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51662 1230 3 Case Labeling

Label for LIDOCAINE HCl Injection USP 1%, 50 mg/5 mL (10 mg/mL) in 5 mL syringes, box of 10, by HF Acquisition Co. LLC. Includes drug facts such as NDC 51662-1230-3, lot number 123456, and expiration date 2030-01-01. The label details product sterile status, storage instructions, and contents including 10 mg lidocaine hydrochloride and 7 mg sodium chloride per mL.*

FDA Label Image

51662 1230 3 Rfid Hf Label Image (2)

A white adhesive label on a white package contains a GS1 DataMatrix barcode and various pharmaceutical product identifier numbers, including a serial number, lot number, and expiration date. Text below instructs to see the manufacturer's package insert and identifies distribution by HF Acquisition Co., LLC, Mukilteo, WA 98275. "RX ONLY" is printed vertically on the right side.*

FDA Label Image

Syringe Label (5ml Syringe Label)

Label for 1% Lidocaine HCl Injection, USP, 50 mg/5 mL, single-dose vial. The label shows product strength, dosage form, volume (5 mL), and includes manufacturer information from Hospira, Inc., Lake Forest, IL. The label also displays an approximate measurement scale in milliliters and a barcode.*

FDA Label Image

Availability (Availability)

A table displaying concentration and pH values for Lidocaine Hydrochloride solutions. It lists formulations for direct intravenous injection and single-dose, showing volumes of 5 mL with total Lidocaine HCl amounts of 100 mg and 50 mg, Lidocaine Hydrochloride concentrations of 20 mg/mL and 10 mg/mL, and pH ranges from 5.0 to 7.0.*

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How Supplied (How Supplied)

Table listing NDC numbers, container types, concentrations, sizes, and total milligrams for LIDOCAINE HCl single-dose injections for direct intravenous use. Containers include Ansyr Plastic Syringe and LifeShield Abboject Syringe with Male Luer Lock Adapter. Concentrations are 1% (10 mg/mL) and 2% (20 mg/mL), all in 5 mL sizes.*

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Logo (Logo)

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Structure (Structure)

Chemical structure of lidocaine hydrochloride monohydrate shown as a molecular diagram with a benzene ring, methyl groups, and amide side chain including hydrochloride and water of hydration.*

* 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.