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

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 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)

Kcl-for-os-30s-carton-labl (Kcl For Os 30s Carton Labl)
Potassium Chloride for Oral Solution, USP 20 mEq Orange Flavored packaging label for 30 single-dose pouches of 1.5 g each. The label shows the NDC 70069-823-30 and notes that the product is Rx only. It is manufactured by Somerset Therapeutics, LLC and includes preparation instructions to dissolve one pouch in 4 ounces of cold water along with storage and caution information.*
FDA Label Image

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

Kcl-for-os-carton-labl (Kcl For Os Carton Labl)
Potassium Chloride for Oral Solution, USP 20 mEq, orange flavored, in a cardboard carton packaging. The package contains 100 single-dose pouches of 1.5 g each. The label shows the product name and strength prominently, with the manufacturer listed as Somerset Therapeutics LLC. Additional text includes dosage and storage instructions, as well as a barcode and NDC 70069-823-10.*
FDA Label Image

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

Kcl-for-os-pouch-labl (Kcl For Os Pouch Labl)
Label for Potassium Chloride for Oral Solution, USP, 20 mEq strength in single-dose 1.5 g orange-flavored pouches. The label includes preparation instructions to dissolve one pouch in 4 ounces of water, cautions, and manufacturing information showing Somerset Therapeutics LLC as the labeler and Granules Pharmaceuticals Inc. as the manufacturer.*

* 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.