Visipaque Injection, Solution
Product Images NDC 0407-2222

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Visipaque (NDC 0407-2222). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Ge Healthcare 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

Chemical Structure (Visipaque 01)

Chemical Structure (Visipaque 01)
Chemical structure of the active ingredient in Visipaque 270 mg/mL, showing its molecular composition and arrangement of atoms including iodine atoms, amide groups, and hydroxyl groups.*
FDA Label Image

Principal Display Panel (270 mgI/mL Bottle Box Label)

Principal Display Panel (270 mgI/mL Bottle Box Label)
Visipaque 270 mg/mL Injection label from GE Healthcare Inc. The label indicates iodixanol as the active ingredient in a sterile aqueous single-dose injection provided in a 10 x 100 mL bottle pack using PlusPak polymer bottles. The packaging includes safety information, barcode, and storage instructions, with a product NDC of 0407-2222.*
FDA Label Image

Principal Display Panel (320 mgI/mL Bottle Box Label)

Principal Display Panel (320 mgI/mL Bottle Box Label)
Label for Visipaque 320 mg iodine/mL (iodixanol) Injection by GE Healthcare Inc. The label indicates single-dose 100 mL bottles in a 10-pack with PLUSPAK polymer bottles. It is for intra-arterial and intravenous use only. The product is sterile aqueous solution, not for intrathecal use. Additional handling and storage instructions are included along with distribution details and a barcode.*

* 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.