Structural Formula Dextrose (Potassium 01)
Potassium Chloride In Dextrose And Sodium Chloride Injection, Solution
Product Images NDC 0990-7903
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Product Visual Gallery
This gallery contains 9 technical images submitted to the FDA as part of the official labeling for Potassium Chloride In Dextrose And Sodium Chloride (NDC 0990-7903). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.
As provided by Icu Medical Inc., these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.
Product Images & Figures Index
Principal Display Panel (1000 mL Bag Label)
This is a description of a prescription medication in the form of an injection. The medication is called 20 mEq POTASSIUM and comes in a 1000 mL container with the NDC number 0990-7107-09. It contains POTASSIUM CHLORIDE, 5% Dextrose, and 0.9% Sodium Chloride. One hundred milliliters of the medication contains POTASSIUM CHLORIDE 149 mg, SODIUM CHLORIDE 900 mg, DEXTROSE, HYDROUS 5 g IN WATER FOR INJECTION. The pH of the medication is adjusted using HCI. The medication is sterile and nonpyrogenic, and it should only be used for intravenous use. The medication should not be used in series connections. The medication should be used according to the instructions in the insert and must be clear and undamaged for use. Consult a pharmacist if necessary, and use aseptic techniques when introducing additives.*
Principal Display Panel (1000 mL Bag Label)
This is a description of an intravenous solution in a single-dose container containing 40 mEq of Potassium Chloride, Sodium Chloride and Dextrose in water for injection. It may contain HCI for pH adjustment and is sterile and nonpyrogenic. The usual dosage is outlined in the insert, and it must not be used in series connections. Additives may be incompatible so consult with the pharmacist first, and when introducing additives, use aseptic technique and do not store. It is for Rx only and contains DEHP. It is produced by ICU Medical, Inc.*
Principal Display Panel (1000 mL Bag Label)
This is a description of a solution used for intravenous administration containing 30 milliequivalents of potassium chloride in 1000 milliliters of 5% dextrose and 0.45% sodium chloride. Each 100 milliliters of the solution contains 224 mg of potassium chloride, 450 mg of sodium chloride, and 5 g of dextrose. Hydrochloric acid may be introduced to adjust the pH of the solution. The solution also contains 77 milliequivalents of sodium and 107 milliequivalents of chloride per 1000 milliliters. It is sterile, nonpyrogenic, and for single-dose use only. The solution should not be used in series connections and additives may be incompatible. Consult a pharmacist when introducing additives, use aseptic technique, mix thoroughly and do not store. The usual dosage is provided in the insert.*
Principal Display Panel (1000 mL Bag Label)
This is a description of a sterile, nonpyrogenic, single-dose injection solution containing 40 mEq of potassium chloride, 450 mg of sodium chloride, and 5 g of dextrose in water for injection. The solution may contain hydrochloric acid for pH adjustment and has a calculated osmolarity of 487 mOsmol/liter. It is intended for intravenous use and additives should be mixed thoroughly and used only with aseptic techniques. The container should not be used if damaged, and the solution must not be used in series connections. Dosage instructions are included within the package.*
Principal Display Panel (1000 mL Bag Label)
This is a description of a solution for intravenous use containing potassium chloride in combination with Dextrose, Sodium Chloride, and Hydrochloride. Each 100 ml contains 745 mg of Potassium Chloride. It has 10 mEq of Potassium, 77 mEq of Sodium, and 87 mEq of Chloride per 1000ml. The solution has a pH of 4.2 and a sterility, nonpyrogenic. The container is for single-use, and it should not be used in series connections. It contains DEHP. The usual dosage information is available in the insert. It is recommended to consult with a pharmacist as additives may be incompatible, and aseptic technique should be used when introducing additives, mixing thoroughly, and not storing.*
Principal Display Panel (1000 mL Bag Label)
This is a description of a medication that is an injection solution called "Potassium Chloride in 5% Dextrose and 0.225% Sodium Chloride Injection, USP". It is available in a single-dose container for intravenous use and contains potassium chloride, sodium chloride, and dextrose hydrated in water for injection. The pH may be adjusted using HCI. The electrolytes per 1000 mL (excluding ions for pH adjustment) are 20 mEq potassium, 38.5 mEq sodium, and 58.5 mEq chloride. This medication should not be used in series connections and may contain additives that are incompatible. The usual dosage is specified in the insert, and it should only be used if the solution is clear and the container is undamaged.*
Principal Display Panel (500 mL Bag Label)
This is a description of an intravenous solution containing 10 mEq of potassium, potassium chloride, sodium chloride, and dextrose in water for injection. It is in a 500 mL single-dose container and is sterile and non-pyrogenic. The electrolytes per 1000 mL include 20 mEq of potassium, 77 mEq of sodium, and 97 mEq of chloride. It is important to consult with a pharmacist before introducing any additives, and to use aseptic technique when mixing and not to store the solution. The usual dosage can be found on the insert, and the solution must not be used if the container is damaged.*
Principal Display Panel (Overwrap)
This text appears to be instructions for opening and handling a medical container. It advises not to remove the overwrap until ready for use and to check for leaks before use. It also gives recommendations for storage and warns against excessive heat and freezing. There is likely an insert included for further information.*
* 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.
