Lidocaine Hci Injection, Solution
Product Images NDC 51662-1233

10 FDA label images from Hf Acquisition Co Llc, Dba Healthfirst · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 10 technical images submitted to the FDA as part of the official labeling for Lidocaine Hci (NDC 51662-1233). 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 Healthfirst, 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

51662-1233-2 Serialized Pouch Labeling (00351662123324 Lidocaine Pouch Label)

51662-1233-2 Serialized Pouch Labeling (00351662123324 Lidocaine Pouch Label)
Label for 2% Lidocaine HCl Injection, USP 100 mg/5 mL (20 mg/mL) 5 mL vial, with NDC 51662-1233-2. The label includes lot number 12345 and an expiration date of 2025-01-01. It notes the drug is for infiltration and nerve block including epidural and caudal use, with storage instructions and manufacturer information for HF Acquisition Co., LLC.*
FDA Label Image

Rfid Labeling (00351662123331 Lidocaine Rfid Label)

Rfid Labeling (00351662123331 Lidocaine Rfid Label)
A small white label featuring a GS1 DataMatrix barcode and associated numeric codes, including a GTIN (00351662123331). The label instructs to see the manufacturer's package insert and states distribution by HF Acquisition Co., LLC in Mukilteo, WA. The text "RX ONLY" is visible vertically on the right side of the label.*
FDA Label Image

Case Labeling (00351662123331 Lidocaine Case Label)

Case Labeling (00351662123331 Lidocaine Case Label)
Label for Lidocaine HCl Injection, USP 2% (20 mg/mL) in a 5 mL vial, box of 20. The label includes NDC 51662-1233-3, lot number 12345, and expiration date 2025-01-01. Manufactured by HF Acquisition Co LLC, Mukilteo, WA 98275. The label notes use for infiltration and nerve block including epidural and caudal administration.*
FDA Label Image

How Supplied (How Supplied)

How Supplied (How Supplied)
A data table showing unit of sale and concentration for Lidocaine HCI injection solution. It lists NDC 0409-2066-05 with a 2% concentration, carton quantities of 10 containing 100 mg/5 mL each, and single-dose vial concentration of 20 mg/mL.*
FDA Label Image

Logo 2 (Logo Spl 2)

FDA Label Image

Logo (Logo Spl)

FDA Label Image

Serialized 5ml Vial Labeling (Serialized Labeling)

Serialized 5ml Vial Labeling (Serialized Labeling)
Vial of 2% Lidocaine HCl Injection, USP, 100 mg/5 mL (20 mg/mL) Solution for Injection. The clear glass vial features a gray flip-off cap and a detailed product label indicating its preservative-free single-dose vial. The label notes the uses for infiltration and nerve block, including epidural and caudal administration. Distributed by HF Acquisition Co., LLC.*
FDA Label Image

Structure (Structure)

Structure (Structure)
Chemical structure diagram of lidocaine hydrochloride showing its molecular composition including aromatic ring and various functional groups.*
FDA Label Image

Dosage (Table 1)

Dosage (Table 1)
A data table titled 'Recommended Dosages Lidocaine Hydrochloride Injection (without epinephrine)' listing lidocaine concentrations (%), volume ranges (mL), and total dose ranges (mg) for various procedures including infiltration (percutaneous, intravenous regional), peripheral nerve blocks (brachial, dental, intercostal, paravertebral, pudendal, paracervical), sympathetic nerve blocks (cervical, lumbar), central neural blocks epidural, thoracic and lumbar analgesia and anesthesia, and caudal obstetrical analgesia and surgical anesthesia.*
FDA Label Image

5ml Vial Label (Vial Label)

5ml Vial Label (Vial Label)
Label for 2% Lidocaine HCl Injection, USP, 100 mg/5 mL (20 mg/mL) preservative-free solution in a 5 mL single-dose vial. The label states it is for infiltration and nerve block, including epidural and caudal use. Distributed by Hospira, Inc., Lake Forest, IL, USA, with instructions for storage and pH adjustment details.*

* 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.