Potassium Chloride Solution
Product Images NDC 27808-169

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Potassium Chloride (NDC 27808-169). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Tris Pharma 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

10% Label (Potassium Chloride Oral Solution 1)

This is a potassium chloride oral solution that needs to be diluted before administration. It comes in a 16 oz (473 mL) container and is a Rx only medication. Each 15 L (tablespoon) contains 20 mEg of potassium chloride, USP. It also contains several inactive ingredients. Dosage and administration instruction should be consulted for proper use. It should be kept out of reach of children and stored at a controlled room temperature. This medication should be protected from light and freezing and dispensed in a defined container. It is manufactured by "s Pharma, Inc." and the product code is LB8650 Rev.00 0172022.*

FDA Label Image

20% Label (Potassium Chloride Oral Solution 2)

This is a description of a medication for oral solution consisting of Potassium Chloride USP, with inactive ingredients such as Glycerin, Sucralose, and others. It is used to treat potassium deficiencies in the body and should be kept out of reach of children. The medication should be stored at a temperature between 15°C to 30°C and dispensed in a tight, light-resistant container. The manufacturer is 's Pharma, Inc.' located in Monmouth Junction. The dosage and administration of the medication are detailed in the accompanying prescription information.*

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