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This is a description of a Sodium Fluoride F-18 Injection, USP used for diagnostic purposes through intravenous administration. Each mL of the injection contains 10 to 200mCilmL of no-carrier added sodium Fluoride in an aqueous 0.9% sodium chloride solution, which should be used within 12 hours of End of Synthesis. The injection is sterile, non-pyrogenic, and comes in a 30 mL multiple-dose vial. Aseptic techniques should be used to handle the dose, and it should not be used if cloudy or if it contains particulate matter. The correct dosage can be calculated from the date and time of calibration. The injection should be stored at 25°C with permitted excursions to 15-30°C in a shielded container. The manufacturer of the injection is Cardinal Health 414, LLC.*
