Potassium Chloride Powder, For Solution
Product Images NDC 53041-420

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 (NDC 53041-420). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Guardian Drug Company, 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-100ct-gdc-carton.jpg (Kcl 100ct Gdc Carton)

Kcl-100ct-gdc-carton.jpg (Kcl 100ct Gdc Carton)
Packaging label for Potassium Chloride for Oral Solution, USP 20 mEq powder for solution by Guardian Drug Company. The label includes dosing information, directions for dilution, storage instructions, and indicates 100 single-dose pouches of 1.5 g potassium chloride each. It is orange flavored and for oral use only.*
FDA Label Image

Kcl-30ct-gdc-carton.jpg (Kcl 30ct Gdc Carton)

Kcl-30ct-gdc-carton.jpg (Kcl 30ct Gdc Carton)
Packaging label for Potassium Chloride for Oral Solution USP 20 mEq powder for solution, orange flavored, by Guardian Drug Company. The label states 30 single-dose pouches with 1.5 g of potassium chloride per pouch, intended for prescription use only. Manufacturer and serialization information are also shown.*
FDA Label Image

Kcl-gdc-pouch.jpg (Kcl Gdc Pouch)

Kcl-gdc-pouch.jpg (Kcl Gdc Pouch)
Packaging label of Potassium Chloride for Oral Solution, USP 20 mEq Single Dose (1.5 g) powder for solution, manufactured by Guardian Drug Company. The label includes NDC 53041-420, usage instruction as Rx only, a barcode, lot and expiration date placeholders, and handling/storage information.*

* 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.