Mannitol Injection, Solution
Product Images NDC 0990-7715

This is a description of a 250 mL container of 20% Mannitol Injection, USP, manufactured by 1CU Medical Inc., containing 50 g/250 mL (200 mg/mL) of mannitol. Each 100 mL of the injection contains 20 grams of mannitol and may contain sodium bicarbonate for pH adjustment. The solution is sterile and nonpyrogenic, and is for intravenous use only. Additives may be incompatible, so users should consult with a pharmacist, if available, and mix the additives thoroughly and aseptically. The solution should be administered intravenously within a specific range of temperature and should be discarded if unused. If the solution is not clear, the container is damaged or crystals form, the solution should not be used. The container is a single-dose container and must not be used in series connections. The text contains a warning about contraindication in severe renal impairment.*

This is a description of 20% Mannitol Injection, USP contained in a single-dose container of 500mL for intravenous use. It contains Mannitol at a concentration of 200mg/mL with sodium bicarbonate for pH adjustment. Each 100mL contains 20 grams of Mannitol. The solution is sterile, non-pyrogenic, and has a calculated osmolality of 1098 mOsmol/L. It is indicated for use with careful inspection and must not be used in series connections. If crystals form, the solution should be agitated to dissolve and administered intravenously at 30 to 37 °C (86 to 986 °F). The solution may have incompatibilities with additives, and it is recommended to consult with a pharmacist when introducing additives to the solution. The dosage information can be found in the insert, and this solution is contraindicated in severe renal impairment.*