Potassium Chloride In Sodium Chloride Injection, Solution
Product Images NDC 0990-7115

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Potassium Chloride In Sodium Chloride (NDC 0990-7115). 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.

FDA Label Image

Principal Display Panel (20 mEq Bag Label)

Principal Display Panel (20 mEq Bag Label)
This is a 1000 mL injection solution containing 20 mEq Potassium Chloride and 174 mEq Sodium Chloride in 0.9% solution for IV use only. It is a sterile, non-pyrogenic solution and should be used only if the solution is clear and container is undamaged. The usual dosage should be consulted with the insert, and sterile, aseptic technique should be used with additives as they may be incompatible. The container must not be used in series connections, and it contains DEHP.*
FDA Label Image

Principal Display Panel (40 mEq Bag Label)

Principal Display Panel (40 mEq Bag Label)
This is a description of a medication called POTASSIUM CHLORIDE in 0.9% Sodium Chloride Injection, USP. This medication comes in a 1000 mL container and each 100 mL of it contains 298 mg of POTASSIUM CHLORIDE and 900 mg of SODIUM CHLORIDE in 5 WATER FOR INJECTION. The electrolytes present in 1000 mL of this medication are 40 mEq of POTASSIUM, 194 mEq of CHLORIDE, and 154 mEq of SODIUM. The medication is sterile, non-pyrogenic, and single-dose for intravenous use only. It also warns to use only if the solution is clear and the container is undamaged, must not use it in series connections, and that additives may be incompatible. When introducing additives, it requires using aseptic technique, mix thoroughly, and not store. The usual dosage is not mentioned in the text.*
FDA Label Image

Principal Display Panel (1000 mL Bag Pouch)

Principal Display Panel (1000 mL Bag Pouch)
This is a set of instructions for using a container of some sort of solution. It includes a warning not to remove the overwrap until ready to use, checking for leaks before use, and recommended storage conditions. However, it is not clear what type of solution or container this text is referring to.*

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