Sodium Fluoride F 18 Injection
Product Images NDC 67939-020

2 FDA label images from The University Of Utah Dba Cyclotron Radiochemistry Lab Huntsman Cancer Institute · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Sodium Fluoride F 18 (NDC 67939-020). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by The University Of Utah Dba Cyclotron Radiochemistry Lab Huntsman Cancer Institute, 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

Sodiumfluorideouterpackaginglabel (Sodiumfluorideouterpackaginglabel)

Sodiumfluorideouterpackaginglabel (Sodiumfluorideouterpackaginglabel)
Label for Sodium Fluoride F18 Injection, USP 200 mCi/mL diagnostic intravenous injection. The label includes NDC 67939-020-10, dosage form details, storage instructions at 25°C, and radioactive material caution. It is manufactured by The University of Utah DBA Cyclotron Radiochemistry Lab Huntsman Cancer Institute. The vial is a 30 mL multiple-dose container with details for use and expiration.*
FDA Label Image

Sodiumfluorideviallabe (Sodiumfluorideviallabel)

Sodiumfluorideviallabe (Sodiumfluorideviallabel)
Label for Sodium Fluoride F 18 Injection, USP, available as 10 to 200 mCi/mL for intravenous diagnostic use. The label includes storage instructions for a 30 mL multiple-dose vial, manufacturing details by The University of Utah Cyclotron Radiochemistry Lab, and a caution for radioactive material. It provides fields for batch number, end of synthesis date/time, activity, concentration, volume, and expiration date/time.*

* 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.