Product Images Potassium Chloride

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Product Label Images

The following 6 images provide visual information about the product associated with Potassium Chloride NDC 63323-669 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.

Structural Formula - pot0c 0002 01

Structural Formula - pot0c 0002 01

Fresenius Kabi Logo - pot0c 0002 02

Fresenius Kabi Logo - pot0c 0002 02

PACKAGE LABEL - PRINCIPAL DISPLAY – Potassium Chloride in 5% Dextrose Injection, USP 10 mEq/L Bag Label - pot0c 0002 03

PACKAGE LABEL - PRINCIPAL DISPLAY – Potassium Chloride in 5% Dextrose Injection, USP 10 mEq/L Bag Label - pot0c 0002 03

PACKAGE LABEL - PRINCIPAL DISPLAY – Potassium Chloride in 5% Dextrose Injection, USP 10 mEq/L Shipper Label - pot0c 0002 04

PACKAGE LABEL - PRINCIPAL DISPLAY – Potassium Chloride in 5% Dextrose Injection, USP 10 mEq/L Shipper Label - pot0c 0002 04

This is a description of a pharmaceutical product with the National Drug Code (NDC) 63323-667-10 667110. The product contains 10 milliequivalents of Potassium Chloride in a 5% Dextrose Injection, USP. It is manufactured and stored by KABI in Lake Zurich, IL 60047. Additionally, it is made in Norway. The product should be kept at a temperature of 20° to 25°C (68° to 77°F) and must be protected from excessive heat. The rest of the text is not legible.*

PACKAGE LABEL - PRINCIPAL DISPLAY – Potassium Chloride in 5% Dextrose Injection, USP 20 mEq/L Bag Label - pot0c 0002 05

PACKAGE LABEL - PRINCIPAL DISPLAY – Potassium Chloride in 5% Dextrose Injection, USP 20 mEq/L Bag Label - pot0c 0002 05

This is a description of a medication in the form of an injection with the brand name "Free Flex." The medication has a National Drug Code of 63323-669-01 and is in a 1000 mL container. It is intended for intravenous use only and requires a prescription. The medication contains 20 mEq of potassium chloride in 5% Dextrose Injection, USP. The electrolytes per 1000 mL are 20 mEq of potassium and 20 mEq of chloride. The container is a single-dose container and any unused portion should be discarded. It is not recommended to administer the medication simultaneously with blood. The usual dosage should be determined by the package insert. The overwrap acts as a moisture barrier. The medication should be used immediately once removed from the overwrap and stored at 20° to 25°C (68° to 77°F). The container closure is made without natural rubber latex and is sterile. The medication is manufactured for Fresenius Kabi and made in Norway. The website for the company is www.fresenius-kabi.com/us.*

PACKAGE LABEL - PRINCIPAL DISPLAY – Potassium Chloride in 5% Dextrose Injection, USP 20 mEq/L Shipper Label - pot0c 0002 06

PACKAGE LABEL - PRINCIPAL DISPLAY – Potassium Chloride in 5% Dextrose Injection, USP 20 mEq/L Shipper Label - pot0c 0002 06

This is a description of a medication named Potassium Chloride meant for injection. The medicine is found in a package containing 10 packs of 1000 mL. The prescription label features the drug's National Drug Code number, dosage, and appropriate storage. There is information about the manufacturer and a batch number. The medication is meant to be kept in a controlled temperature environment and away from excessive heat. The medication is intended to be administered intravenously to provide Potassium Chloride to the body.*

* 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.