Product Images Potassium Chloride In Dextrose And Sodium Chloride

This is a description of a 1000 mL sterile, non-pyrogenic single dose container of 0.15% Potassium Chloride in 5% Dextrose and 0.20% Sodium Chloride Injection USP, with an EXCEL® container. The solution has a pH of 4.4 (3.5-6.5) and a calculated osmolarity of 360 mOsmol/liter, which is hypertonic. It is recommended for intravenous use only after checking the solution is clear, and container and seals are intact. It should be stored at room temperature not to exceed 25°C to avoid excessive heat and protect from freezing. The solution contains Hydrous Dextrose USP 5 g, Sodium Chloride USP 0.20 g, and Potassium Chloride UPS 1.5 g with electrolytes (mEq/liter): Na* 34; K* 20; CI” 54. It is not made with natural rubber latex, VC, or DEHP. The package is distributed by B. Braun Medical Inc., Pennsylvania, USA.*

This is a description of a medical solution known as Potassium Chloride in 5% Dextrose and 0.20% Sodium Chloride Injection USP, which is mainly used for treating patients who have an electrolyte imbalance. It is available in a 250ml container with a barcode and an expiration lot number, and contains 20 mEq K* per liter. The solution has a specific osmolarity of 360 mOsmalfter ypertec, and has a particular combination of sodium, potassium, and other ions measured in milliequivalents per liter. Because of its composition, it should not be mixed with certain incompatible solutions.*

This is a description of a sterile, nonpyrogenic solution that is used intravenously. It contains 0.15% Potassium Chloride, 5% Dextrose, and 0.9% Sodium Chloride. This solution is hypertonic and has a pH of 4.4 (3.5-6.5). It is an electrolyte solution with Na* 154; K* 20; CI”174 (mEqfiter). It comes in a single dose container and should not be used in series connection. It should be used only if the solution is clear and the container and seals are intact. This solution should be stored at room temperature and protected from freezing. The solution is not made with natural rubberfatex, VC or DEHP.*

This is a description of an injection solution with the following components: 0.15% Potassium Chloride, 5% Dextrose, and 0.33% Sodium Chloride. The container has a volume of 1000mL and is a single-dose container. The electrolytes included are: Na (56mEq/L), K (20mEq/L), and CI (76mEq/L). The solution is sterile, non-pyrogenic, and for intravenous use only. It has a pH of 4.4 and hypertonic with calc. osmolarity of 405 mOsmol/L. The solution should not be used in a series connection and must only be used if the solution is clear, and the container and seals are intact. Additionally, the solution should be mixed thoroughly and additives should only be introduced using aseptic techniques. The solution should be stored at room temperature and protected from excessive heat and freezing. The product is not made with natural rubber latex, VC or DEHP. The product is registered under the trademark EXCEL from B, Braun Medical Inc. If the solution has minute leaks, it must be discarded as it may impair sterility. The solution is available in the USA and Canada.*

This is a description of a sterile intravenous solution called 0.075% Potassium Chloride in 5% Dextrose and 0.45% Sodium Chloride. It contains 10 mEq K*/liter and electrolytes such as Na, K, and CI. The solution is meant for intravenous use only and is stored at room temperature. It is important to check for leaks before use, and the solution should be discarded if any are found. The container is a single-use container and is not made with natural rubber latex, PC, or DEHP. The brand of the container is Excel.*

This is a description of a intravenous solution used for electrolyte replenishment. The solution contains 0.15% potassium chloride, 5% hydrous dextrose, and 0.45% sodium chloride in a 1000 mL EXCEL container. Each 100 mL of the solution contains 77 mEq/L sodium, 20 mEq/L potassium, and 97 mEq/L chloride. It is a single-dose container and should not be used in series connection. The solution is sterile, nonpyrogenic, and hypertonic. It is recommended to store the solution at room temperature, avoiding excessive heat and freezing. The container and seals should be checked for integrity before use. The solution should not be used if the container is damaged or the solution is not clear. It is important to consult with a pharmacist before introducing additives and to use aseptic techniques. Additionally, it should be noted some additives may be incompatible with this solution. The container is not made with natural rubber latex, PVC, or DEHP. The product is labeled for prescription use only, and it is made and distributed by B. Braun Medical Inc.*

This is a description of a 1000 mL intravenous solution of 0.22% Potassium Chloride, 5% Dextrose, and 0.45% Sodium Chloride. It is a single-dose container for intravenous use only that should not be used in series. The solution should be used if the container is intact and the solution is clear. It is advised not to add incompatible additives and to use aseptic techniques if adding additives, mixing them thoroughly, and discarding the solution if minute leaks are found when squeezing the container. The solution is sterile, non-pyrogenic, and is stored at room temperature. The overwrap should not be removed until it is ready to use. The solution does not contain natural rubber latex, PVC, or DEHP.*

This is a description of a medical solution containing 0.30% potassium chloride, 5% dextrose, and 0.45% sodium chloride. It is intended for intravenous use, and each 100 mL contains hydrous dextrose, sodium chloride, potassium chloride, and water for injection. This solution is sterile, nonpyrogenic, and comes in a single dose container. The solution has a pH of 4.4 and a calculated osmolarity of 490 mOsmol per liter, which is hypertonic. However, it is warned that some additives may be incompatible with the solution. The recommended storage for the solution is at room temperature, and it should be protected from freezing. The package insert should be reviewed for additional information.*