Gastrografin Liquid
Product Images NDC 0270-0445

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Gastrografin (NDC 0270-0445). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Bracco Diagnostics 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

Gastrografin Label 12x120 (Gastrografin Label 12x120ml)

Gastrografin oral and rectal liquid containing diatrizoate meglumine and diatrizoate sodium solution USP with strengths of 660 mg/mL and 100 mg/mL. The label indicates it is a bulk container with 12 bottles of 120 mL each, manufactured by Bracco Diagnostics Inc. Includes handling instructions, storage conditions, and barcode.*

FDA Label Image

Gastrografin Label 120ml (Gastrografin Label Internal 120ml)

Gastrografin 37% Organically Bound Iodine liquid, containing diatrizoate meglumine and diatrizoate sodium solution USP, labeled for oral or rectal use in a 120 mL single dose bottle. The label highlights the active ingredients and warns with a prominent 'DO NOT INJECT' statement in red. Manufactured by Bracco Diagnostics Inc, the label includes storage instructions, usage directions, and the NDC code 0270-0445-40.*

FDA Label Image

Gastrografin Structure (Gastrografin Structure)

Chemical structure diagrams of diatrizoate meglumine and diatrizoate sodium, including their molecular formulas, molecular weights, organic iodine percentages, and CAS numbers, as labeled in the image.*

* 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.