Fludeoxyglucose F 18 Injection, Solution
Product Images NDC 76318-334

3 FDA label images from Massachusetts General Hospital · 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 Fludeoxyglucose F 18 (NDC 76318-334). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Massachusetts General Hospital, 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

Vial Label (Fdg Vial Label)

Vial Label (Fdg Vial Label)
Fludeoxyglucose F18 Injection vial label showing concentration range from 20 mCi/mL to 300 mCi/mL at End of Synthesis. The label includes lot number space and cautions about radioactive material from Massachusetts General Hospital PET Center, Boston, MA. It also features a radiation hazard symbol and a warning against use if cloudy or containing particulates.*
FDA Label Image

Chemical Structure (Fdg)

Chemical Structure (Fdg)
Chemical structure of Fludeoxyglucose F-18, showing the arrangement of atoms including fluorine-18, hydroxyl groups, and other bonded elements in the molecular structure.*
FDA Label Image

Lead Shield Label (Fdgsafelabel)

Lead Shield Label (Fdgsafelabel)
Label for Fludeoxyglucose F-18 Injection 300 mCi/mL, an intravenous solution for diagnostic use. The label includes space for batch number, calibration date/time, activity, concentration, volume, and expiration details. It states radioactive material caution, storage instructions at 25°C, and manufacturer Massachusetts General Hospital PET Center. The label also notes the 18F half-life and expiration 12 hours after synthesis.*

* 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.