Freeflex Logo (Pot0d 0004 01)
Potassium Chloride Injection
Product Images NDC 65219-008
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 65219-008). 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.*
* 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.
