Potassium Chloride Powder, For Solution
Product Images NDC 72603-407

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Potassium Chloride (NDC 72603-407). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Northstar Rx 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

Image Description (Potassium Chloride Oral Solution 1pt5mg 100s Carton Label)

Potassium Chloride for Oral Solution, USP 20 mEq powder for solution label. The packaging indicates each pouch contains 1.5 g of potassium chloride with 100 single-dose pouches per package. Manufactured by Northstar Rx LLC, the label includes dosage preparation instructions and storage conditions. The product is for oral use and labeled Rx Only.*

FDA Label Image

Image Description (Potassium Chloride Oral Solution 1pt5mg 30s Carton Label)

The image shows the packaging label for Potassium Chloride for Oral Solution USP, 20 mEq, in powder form. The label indicates each pouch contains 1.5 g potassium chloride. The package includes 30 single-dose pouches. The labeler is Northstar Rx LLC. Usage instructions and storage information are also present, along with barcodes and manufacturing details.*

FDA Label Image

Image Description (Potassium Chloride Oral Solution 1pt5mg Pouch Label)

Label for Potassium Chloride for Oral Solution USP 20 mEq single dose (1.5 g) powder for solution by Northstar Rx LLC. The label includes the NDC 72603-407-01, Rx Only designation, manufacturer details, barcode, and storage instructions. The label is designed with blue, white, and purple colors, including the NorthStar logo.*

* 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.