Omnipaque Injection, Solution
Product Images NDC 0407-1413

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Omnipaque (NDC 0407-1413). 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 (Omnipaque 01)

Chemical structure diagram of the active ingredient likely related to Omnipaque, showing a benzene ring with iodine atoms and several functional groups attached, including hydroxyl and amide groups.*

FDA Label Image

Principal Display Panel (300 mg Iodine/mL Bottle Box Label)

Label for Omnipaque 300 mg iodine/mL (iohexol) injection by GE Healthcare, for intravenous use. The label states it contains 10 x 500 mL bottles. Use is specified for imaging bulk package or pharmacy bulk package with restrictions for direct infusion, including intrathecal, intra-arterial, intravenous, oral, rectal, intraarticular, or body cavity uses. Storage and handling instructions, ingredients, and barcodes are present.*

FDA Label Image

Principal Display Panel (350 mg Iodine/mL Bottle Box Label)

Omnipaque 350 mg iodine/mL iohexol injection label by GE Healthcare for 10 x 500 mL bottles. The label states the product can be used either as Imaging Bulk Package for intravenous use only or Pharmacy Bulk Package not for direct infusion, intended for intra-arterial, intravenous, oral, intra-articular, or body cavity use. The label includes storage and usage instructions, barcodes, lot and expiration details, and distributor contact information.*

* 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.