Lidocaine Hcl Injection, Solution
Product Images NDC 51662-1593

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 11 technical images submitted to the FDA as part of the official labeling for Lidocaine Hcl (NDC 51662-1593). 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

D (Description)

D (Description)
Data table comparing lidocaine HCl (anhydrous) and sodium chloride concentrations by percentage. The table shows mg/mL values of lidocaine ranging from 5 to 20 and sodium chloride concentrations decreasing from 8 to 6 as lidocaine concentration increases from 0.5% to 2%.*
FDA Label Image

D1 (Dosage 1)

D1 (Dosage 1)
A data table presenting different Lidocaine HCl injection solution strengths (1%, 1.5%, 2%) alongside their corresponding single-dose packaging formats and volumes, which include 30 mL teartop vials, 20 mL ampuls, and 10 mL ampuls respectively.*
FDA Label Image

D2 (Dosage 2)

D2 (Dosage 2)
A data table titled "Recommended Dosages" for Lidocaine Hydrochloride Injection, USP (without Epinephrine). It lists various medical procedures with corresponding concentration percentages, volume ranges in milliliters, and total dose ranges in milligrams. Procedures include infiltration, peripheral nerve blocks, sympathetic nerve blocks, and central neural blocks with detailed dosage information for each type.*
FDA Label Image

L2 (Logo 2)

FDA Label Image
FDA Label Image

Case Labeling (Lidocaine Case Label)

Case Labeling (Lidocaine Case Label)
Lidocaine HCl Injection, USP 1% 20 mg/2 mL (10 mg/mL) solution in 2 mL ampules, packaged as a case of 50. The label shows the NDC 51662-1593-3, lot and expiration information, and states the solution is preservative-free for infiltration and nerve block including epidural and caudal use. Manufactured by HF Acquisition Co LLC, DBA HealthFirst, Mukilteo, WA.*
FDA Label Image

Pouch Labeling (Pouch 2)

Pouch Labeling (Pouch 2)
Label for Lidocaine HCl Injection USP 1% with 20 mg in 2 mL (10 mg/mL) solution. Includes NDC 51662-1593-2, lot and expiration details, and notes it is preservative-free for epidural and caudal nerve block use. Manufactured by HF Acquisition Co LLC, located in Mukilteo, WA, with an original MFG NDC of 0499-4713-32. The label also contains storage information and a QR code.*
FDA Label Image

Precautions (Precautions)

Precautions (Precautions)
A data table titled 'Examples of Drugs Associated with Methemoglobinemia' listing drug classes and examples. Classes include Nitrates/Nitrites (e.g., nitric oxide, nitroglycerin), Local anesthetics (e.g., lidocaine, articaine), Antineoplastic agents, Antibiotics, Antimalarials, Anticonvulsants, and Other drugs with associated examples under each category.*
FDA Label Image

Rfid Labeling (Rfid 1)

Rfid Labeling (Rfid 1)
LIDOCAINE HCl injection, solution packaging label showing a small white label with barcode and numeric codes. It includes distribution information by HF Acquisition Co LLC, DBA HealthFirst, Mukilteo, WA 98275. The label indicates the product is prescription only (RX ONLY).*
FDA Label Image

Structure (Structure)

Structure (Structure)
Chemical structure diagram of lidocaine hydrochloride, showing the aromatic ring with two methyl groups and attached amide and amine functional groups, along with hydrochloride and water molecules.*
FDA Label Image

Vial Label (Vial 2)

Vial Label (Vial 2)
Label for Lidocaine HCl Injection, USP 20 mg/2 mL (1%), preservative-free solution in a 2 mL vial. The label shows the lot number, barcode, and indicates distribution by Hospira, Inc., Lake Forest, IL, USA. It is marked Rx only.*

* 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.