Potassium Chloride Injection
Product Images NDC 65219-006
View Photos of Packaging, Regulatory Labels, and Product Appearance
Product Visual Gallery
This gallery contains 7 technical images submitted to the FDA as part of the official labeling for Potassium Chloride (NDC 65219-006). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.
As provided by Fresenius Kabi Usa, Llc, these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.
Figure (Pot0d 0004 02)
Package Label (Principal Display Panel)
This is a description for freeflex® Potassium Chloride Injection, a prescription medication, containing 10 mEq per 100 mL of Potassium Chloride to be administered intravenously using calibrated infusion devices. This is a single-dose container, and any unused portion should be discarded. It should only be used with a calibrated infusion device, and supplementary medication should not be added. The usual dosage instructions are provided in the package insert. The medication is stored in a moisture barrier overwrap until ready to use, and it is recommended to store it between 20° to 25°C. The container closure is not made with natural rubber latex, and it is sterile and Non-PVC, Non-DEHP. The medication is manufactured in Norway and distributed by Fresenius Kabi in Lake Zurich, IL.*
Package Label (Principal Display Panel)
This is a description of a medication called free flex® with an NDC number of 65219-004-00. It comes in a single-dose container with a size of 50mL, which contains 10 mEq per 50 mL of Potassium Chloride for intravenous use. The container is hypertonic 400 mOsmol/L and has a pH level of 5 (4 to 8). The medication should be used with a calibrated infusion device and is only for Rx use. The standard dosage must be determined by a physician, and supplementary medication should not be added. The medication should be stored at 20° to 25°C (68° to 77° F) until ready to use. The container does not contain natural rubber latex and is sterile. It is made in Norway for Fresenius in Lake Zurich, IL.*
Package Label (Principal Display Panel)
Package Label (Principal Display Panel)
This is a description of Freeflox® Potassium Chloride Injection, a medication for intravenous use. It comes in a 50 mL single-dose container with each dose containing 20 mEq per 500 mL of Potassium Chloride. It is hypertonic and has a pH level between 4 to 8. The usual dosage is indicated in the package insert. It should be used only with a calibrated infusion device, preferably through a central route. It should be stored in a moisture barrier overwrap and at a temperature of 20 to 25°C. The container closure is free from natural rubber latex and made in Norway with non-PVC and non-DEHP material. It is manufactured for Lake Zurich, IL 60047. No information available about the medication's uses or indications.*
Package Label (Principal Display Panel)
This is a 100 mL single-dose container of Potassium Chloride Injection, with 40 mEq per 100 mL, for intravenous use only. Each 100 mL contains 2.98 g of Potassium Chioride, Potassium 400 mEq/L, Chioride 400 mEq/L, hypertonic 799 mOsmol/L (Calc) pH 5 (4 to 8). It should be used only with a calibrated infusion device and central route whenever possible. Do not add supplementary medication. The usual dosage can be found in the package insert. It is recommended to store it in a moisture barrier overwrap until ready to use, and at 20° to 25°C (68° to 77°F) [see USP Controlled Room Temperature]. The container closure is not made with natural rubber latex and is non-PVC, non-DEHP, and sterile. The manufacturer is Fresenius Kabi, and it was made in Norway.*
* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.