Sodium Polystyrene Sulfonate Powder, For Suspension
Product Images NDC 24658-760

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This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Sodium Polystyrene Sulfonate (NDC 24658-760). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Puracap Laboratories, 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.

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FDA Label Image

L:\labeling Department\anda\sodium Polystyrene Sulfonate_sz- Done\epic\spl\archive\version 7 Sodium Polystyrene\spl\14 (14)

L:\labeling Department\anda\sodium Polystyrene Sulfonate_sz- Done\epic\spl\archive\version 7 Sodium Polystyrene\spl\14 (14)
This text provides information about the dosage and administration of Sodium Polystyrene Sulfonate Powder for Suspension, a prescription medication used to treat patients with high levels of potassium in their blood. The recommended dose for an adult is 15 grams (approximately 4 level teaspoons) dissolved in water, taken one to four times a day. The medication's effect on the body should be monitored closely with frequent potassium level tests. The medication should be stored in a tight, light-resistant container as defined in official compendia and should be used only for 24 hours after preparation. The text also provides the drug's NDC number, manufacturer, and contact information.*
FDA Label Image

Image 01

Image 01

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