Logo (Logo Spl)
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.
Product Images & Figures Index
Structure (Structure)
Chemical structure diagram of lidocaine hydrochloride showing its molecular composition including aromatic ring and various functional groups.*
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.*
Logo 2 (Logo Spl 2)
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.*
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.*
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.*
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.*
Rfid Label (51662 1233 3 Rfid)
A close-up image of a white label affixed to a medication package, showing black printed text and a data matrix barcode. The text includes numeric codes and instructions to see manufacturer's insert. It also mentions the product is distributed by HF Acquisitions Co., LLC in Mukilteo, WA. The packaging is for Lidocaine HCI injection, solution, 20 mg/mL, with labeler HF Acquisition Co LLC, DBA HealthFirst.*
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.*
* 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.
