Lidocaine Hydrochloride Injection, Solution
Product Images NDC 0409-4283

5 FDA label images from Hospira, Inc. · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Lidocaine Hydrochloride (NDC 0409-4283). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Hospira, 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

Hospira Logo (Lidocaine 01)

FDA Label Image

Structural Formula Lidocaine Hydrochloride (Lidocaine 02)

Structural Formula Lidocaine Hydrochloride (Lidocaine 02)
Chemical structure of Lidocaine Hydrochloride, showing the molecular formula with aromatic ring, methyl groups, and hydrochloride and water components.*
FDA Label Image

Hospira Logo (Lidocaine 03)

FDA Label Image

Principal Display Panel (5 mL Ampule Label)

Principal Display Panel (5 mL Ampule Label)
Label for Lidocaine Hydrochloride Injection, USP 4% (200 mg/5 mL or 40 mg/mL) preservative-free solution. The 5 mL single-dose product is indicated for topical use and retrobulbar injection. Distributed by Hospira, Inc., Lake Forest, IL, USA, with NDC 0409-4283-11. Rx only.*
FDA Label Image

Principal Display Panel (5 mL Ampule Cello Pack Label)

Principal Display Panel (5 mL Ampule Cello Pack Label)
Label for Lidocaine HCl Injection, USP, 4% (200 mg/5 mL, 40 mg/mL), preservative-free solution. The product is in 5 single-dose ampuls, labeled for topical use and retrobulbar injection. Manufactured and distributed by Hospira, Inc., the label includes NDC 0409-4283-25 and storage instructions at controlled room temperature.*

* 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.