Product Images Potassium Chloride

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Product Label Images

The following 7 images provide visual information about the product associated with Potassium Chloride NDC 65219-012 by Fresenius Kabi Usa, Llc, such as packaging, labeling, and the appearance of the drug itself. This resource could be helpful for medical professionals, pharmacists, and patients seeking to verify medication information and ensure they have the correct product.

freeflex Logo - pot0d 0004 01

freeflex Logo - pot0d 0004 01

Figure - pot0d 0004 02

Figure - pot0d 0004 02

Package Label - Principal Display Panel - Potassium Chloride 10 mEq 100 mL Bag Label - pot0d 0004 03

Package Label - Principal Display Panel - Potassium Chloride 10 mEq 100 mL Bag Label - pot0d 0004 03

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 - Potassium Chloride 10 mEq 50 mL Bag Label - pot0d 0004 04

Package Label - Principal Display Panel - Potassium Chloride 10 mEq 50 mL Bag Label - pot0d 0004 04

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 - Potassium Chloride 20 mEq 100 mL Bag Label - pot0d 0004 05

Package Label - Principal Display Panel - Potassium Chloride 20 mEq 100 mL Bag Label - pot0d 0004 05

Package Label - Principal Display Panel - Potassium Chloride 20 mEq 50 mL Bag Label - pot0d 0004 06

Package Label - Principal Display Panel - Potassium Chloride 20 mEq 50 mL Bag Label - pot0d 0004 06

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 - Potassium Chloride 40 mEq 100 mL Bag Label - pot0d 0004 07

Package Label - Principal Display Panel - Potassium Chloride 40 mEq 100 mL Bag Label - pot0d 0004 07

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.*

* The product label images have been analyzed using a combination of traditional computing and machine learning techniques. It should be noted that the descriptions provided may not be entirely accurate as they are experimental in nature. Use the information in this page at your own discretion and risk.