Sodium Polystyrene Sulfonate Suspension
Product Images NDC 35573-108

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Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Sodium Polystyrene Sulfonate (NDC 35573-108). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Burel Pharmaceuticals, 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

Chem (Sodium Polystyrene Sulfonate Suspension Usp 1)

FDA Label Image

Carton (Sodium Polystyrene Sulfonate Suspension Usp 2)

Carton (Sodium Polystyrene Sulfonate Suspension Usp 2)
This is a description for a medication named Sodium Polystyrene Sulfonate Suspension, USP. It is used for the treatment of high levels of potassium in the blood.*
FDA Label Image

Pint (Sodium Polystyrene Sulfonate Suspension Usp 3)

Pint (Sodium Polystyrene Sulfonate Suspension Usp 3)
This is a description of a medication called Sodium Polystyrene Sulfonate Suspension, USP, indicated for oral or rectal use. Each 60 mL of the suspension contains 15 g of Sodium Polystyrene Sulfonate USP, along with other ingredients such as Propylene Glycol USP and Xanthan Gum. The sodium content is 1.5 g (65 mEq) in 60 mL. The usual dose should be followed as per the package insert. The medication should be stored at 20°-25°C (68°-77°F) with excursions allowed between 15°-30°C (59°-86°F). It needs to be dispensed in a tight container as per USP standards. This medication is manufactured by Burel Pharmaceuticals LLC in Mason, OH, USA.*

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