Indium Dtpa In 111 Solution
Product Images NDC 17156-251

3 FDA label images from Medi-physics, Inc. Dba Ge Healthcare · 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 Indium Dtpa In 111 (NDC 17156-251). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Medi-physics, Inc. Dba 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.

Product Images & Figures Index

FDA Label Image

Principal Display Panel (1.5 mL Vial Label)

Principal Display Panel (1.5 mL Vial Label)
Label for Indium DTPA In 111 solution, 1 mCi/mL (37 MBq/mL), an intrathecal sterile aqueous solution containing Pentetate Indium Disodium In 111. The label includes storage instructions (store 5°-30°C, do not freeze), expiration time (7 days after calibration), and a caution for radioactive material. Manufactured by GE Healthcare, Medi-Physics, Inc., Arlington Heights, IL, with product NDC 17156-251-08 and volume 1.5 mL (total activity 1.5 mCi).*
FDA Label Image

Graph 1 (Indium Dtpa Image01)

Graph 1 (Indium Dtpa Image01)
A line graph showing percentage values on the vertical axis and time (days) on the horizontal axis, ranging from calibration time to expiration time. It compares two elements, labeled Zn 65 and In 114m, with their values increasing gradually over a 7-day period.*
FDA Label Image

Structural Formula (Indium Dtpa Image02)

Structural Formula (Indium Dtpa Image02)
Chemical structure diagram of Indium In-111 Pentetate Disodium, showing the central indium atom complexed with pentetate (DTPA) and sodium carboxylate groups.*

* 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.