Suprep Bowel Prep Solution, Concentrate
Product Images NDC 24338-175

Product Visual Gallery

This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Suprep Bowel Prep (NDC 24338-175). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Azurity Pharmaceuticals, Inc., 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

K2so4 Structure (K2so4)

Chemical structure of sodium sulfate, illustrating sulfate ion with sulfur atom centrally bonded to four oxygen atoms, two of which carry negative charges, and associated with potassium ions as indicated by "K+" symbols.*

FDA Label Image

Mgso4 Structure (Mgso4)

Chemical structure of magnesium sulfate depicted as a central magnesium ion (Mg2+) coordinated to a sulfate ion (SO4) which includes sulfur bonded to four oxygen atoms.*

FDA Label Image

Na2so4 (Naso4)

Chemical structure diagram of sodium sulfate, potassium sulfate, or magnesium sulfate, showing sulfur, oxygen, sodium, and potassium atoms connected in a sulfate ion arrangement.*

FDA Label Image

Adult-carton (Suprep Carton)

SUPREP Bowel Prep Kit (sodium sulfate, potassium sulfate, magnesium sulfate) oral solution for adults, with a strength of 17.5g/3.13g/1.6g per 6 ounces. The label shows the kit contents, dosage instructions, storage conditions, and mixing instructions. It is manufactured by Azurity Pharmaceuticals, Inc. and includes a barcode and NDC 24338-175-01.*

FDA Label Image

Adult-label (Suprep Label)

Label for SUPREP Bowel Prep Kit oral solution containing sodium sulfate, potassium sulfate, and magnesium sulfate. The label states the product is for adults, lists the contents as 6 ounces (177 mL) of liquid bowel prep with active ingredients totaling 17.5g, 3.13g, and 1.6g per 6 ounces. It provides directions for use, storage instructions, and manufacturer details for Azurity Pharmaceuticals, Inc.*

* 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.