Potassium Chloride In Dextrose And Sodium Chloride Injection, Solution
Product Images NDC 65219-119

Product Visual Gallery

This gallery contains 7 technical images submitted to the FDA as part of the official labeling for Potassium Chloride In Dextrose And Sodium Chloride (NDC 65219-119). 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.

FDA Label Image

Figure (Pot0m 0001 01)

FDA Label Image

Figure (Pot0m 0001 02)

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Fresenius Kabi Logo (Pot0m 0001 03)

FDA Label Image

Package Label (PRINCIPAL DISPLAY – Potassium Chloride in 5% Dextrose and 0.9% Sodium Chloride Injection, USP)

This is a description of a medical product identified by the NDC code 65219-118-01. The product is a 1000 mL IV solution that contains 20 mEq of potassium chloride, sodium chloride, dextrose, and water for injection. The solution has a pH range of 3.5 to 6.5, and should be used immediately after removing the overwrap. The product should be stored between 20°C to 25°C (68°F to 77°F) and protected from freezing. The product is manufactured by Fresenius Kabi in Norway and the container closure is not made with natural rubber latex.*

FDA Label Image

Package Label (PRINCIPAL DISPLAY)

This product is a solution containing Potassium Chloride in 5% Dextrose and 0.9% Sodium Chloride Injection, USP. It is packaged in a 1000 mL bag and is manufactured by Fresenius Kabi for ES. The product is stored at controlled room temperature and should be protected against freezing and excessive heat. The product has an expiration date and lot number printed on the bag.*

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Package Label (PRINCIPAL DISPLAY – Potassium Chloride in 5% Dextrose and 0.9% Sodium Chloride Injection, UPS Bag Label)

This is a description for a solution used for intravenous therapy. It is a single-dose container that should be discarded once unused. The solution contains 40mEg of Potassium and 20mEq of Chloride. It also contains Dextrose Hydrous and two types of salts. The solution is stored between 20° to 25°C and is protected from freezing. The overwrap serves as a moisture barrier, and additives should not be stored after the container is open. The solution is manufactured by Fresenius Kabi, a company based in Norway.*

FDA Label Image

Package Label (PRINCIPAL DISPLAY – Potassium Chloride in 5% Dextrose and 0.9% Sodium Chloride Injection, USP Case Label)

This is a description of a medicine called "Potassium Chloride in 5% Dextrose and 0.9% Sodium Chloride Injection, USP". It comes in a pack of 1000 mL x 10, and the NDC code is 65219-119-10. The medicine should be stored at a temperature of 20° to 25°C (68° to 77°F) and should be protected from freezing and excessive heat. The medicine is manufactured by Fresenius Kabi in Norway, and the pack has an EXP date and LOT number. The text also includes a bar code with the product number and manufacturer name.*

* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.