Product Images Potassium Chloride

This is a prescription medication with the NDC code of 60505-6184-6. It is manufactured by Apotex Corp. and contains 20 mEq of Potassium Chloride USP per 15 mL. The inactive ingredients include citric acid, glycerin, methylparaben, natural orange flavor, propylene glycol, propylparaben, purified water, sodium citrate, and sucralose. The usual dosage is not given and it is recommended to store the medication in a tight, light-resistant container at controlled room temperature. It is important to keep this medication out of the reach of children.*

This is a description of Potassium Chloride Oral Solution USP, a medication used for electrolyte replenishment. It is available in a 473mL bottle with each 15mL containing 40 mEq of Potassium Chloride USP. The medication should be diluted before use and may contain inactive ingredients such as citric acid, FD&G Yellow #6, glycerin, methylparaben, natural orange flavor, propylene glycol, propylparaben, purified water, sodium citrate, dinydrate, and Sucralose. Usual dosage and prescribing information should be checked before use. It should be stored at room temperature and kept in a tight, light-resistant container. The manufacturer is Apotex Inc. and it is distributed by Apotex Corp.*

This is a medication containing potassium chloride used to treat low levels of potassium in the blood. Each 15 mL (tablespoon) contains 40 mEq of potassium chloride USP that needs to be diluted prior to administration. It also contains inactive ingredients such as citric acid, FDAC Yellow #6, glycerin, methylparaben, natural orange flavor (fruit extract and natural flavor), propylene glycol, propylparaben, purified water, sodium citrate dihydrate, and sucralose. The medication needs to be stored at room temperature and dispensed in a tight, light-resistant container separated from light and freezing. It is manufactured by Apota Inc in Toronto, Ontario, Canada, and distributed by Apotex Corp in Weston, FL 33326. No dosage instructions are provided.*