Potassium Chloride For Oral Solution For Solution
Product Images NDC 70069-823

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Potassium Chloride For Oral Solution (NDC 70069-823). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Somerset Therapeutics, 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

Kcl-for-os-30s-carton-labl (Kcl For Os 30s Carton Labl)

This is product information for Potassium Chloride oral solution in single-dose pouches, with each pouch containing 1.5 grams of potassium chloride (KCl). The solution is orange-flavored and provides 20 mEq of potassium and chloride. Dosage should be personalized for each patient. The preparation involves dissolving the pouch contents in 4 ounces of cold water. It must be diluted and stored at 25°C, with excursions allowed between 15° to 30°C. The product is manufactured by Granules Pharmaceuticals Inc. for Somerset Therapeutics LLC.*

FDA Label Image

Kcl-for-os-carton-labl (Kcl For Os Carton Labl)

This is information regarding a medication called Potassium Chloride for Oral Solution, USP in orange flavor. It comes in 100 single-dose pouches, with each pouch containing 1.5g of potassium chloride providing 20 mEq of potassium and chloride. The dosage must be adjusted according to individual patient needs. The medication must be diluted before use and stored at recommended temperatures. Additionally, it was manufactured for Somerset Therapeutics, LLC by Granules Pharmaceuticals Inc. in Chantilly, VA.*

FDA Label Image

Kcl-for-os-pouch-labl (Kcl For Os Pouch Labl)

This text provides information about a potassium chloride oral solution in single-dose pouches. Each pouch contains 1.5g of potassium chloride, which is equivalent to 20 mEq of potassium and 20 mEq of chloride. The product must be diluted before use and should be kept out of reach of children. It is orange flavored and manufactured by Granules Pharmaceuticals Inc. for Somerset Therapeutics LLC in New Jersey. The usual dosage and further details can be found in the prescribing information.*

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