Clariscan Injection, Solution
Product Images NDC 0407-2943

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Clariscan (NDC 0407-2943). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Ge Healthcare, 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

Image (Clariscan 02)

Label for Clariscam (gadoterate meglumine) Injection, a sterile solution for intravenous use with a concentration of 5 mmol per 10 mL (0.5 mmol per mL). The label notes single-dose 10 mL vials, storage instructions, and distribution by GE Healthcare.*

FDA Label Image

Chemical Structure (Clariscan 01)

Chemical structure of gadoterate meglumine, the active ingredient in CLARISCAN injection solution. The diagram shows the gadolinium ion (Gd3+) complexed with a macrocyclic ligand and the meglumine molecule.*

FDA Label Image

Principal Display Panel (10 mL Vial Box Label)

CLARISCAN (gadoterate meglumine) Injection 5 mmol per 10 mL (0.5 mmol per mL) sterile solution for intravenous administration. The label states the concentration as 376.9 mg/mL gadoterate meglumine. Packaged as 10 single-dose 10 mL vials. Distributed by GE Healthcare, Marlborough, MA, USA. Includes storage and handling instructions.*

FDA Label Image

Principal Display Panel (15 mL Syringe Box Label)

Label for Clariscantm (gadoterate meglumine) Injection, 7.5 mmol per 15 mL (0.5 mmol per mL) sterile solution for intravenous administration. The label indicates storage instructions, lot number, expiration date, and that the product is a single-dose 15 mL pre-filled plastic syringe distributed by GE Healthcare. The product is labeled for Rx only and is of Norwegian origin.*

* 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.