Cholestyramine Powder, For Suspension
Product Images NDC 42806-267

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Cholestyramine (NDC 42806-267). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Epic Pharma, 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

Can.jpg (Pouch)

Can.jpg (Pouch)
Label of CHOLESTYRAMINE for oral suspension, USP powder, containing 4 grams of cholestyramine resin per scoopful. It features preparation instructions, a barcode, and warnings including child resistance and storage conditions (20 to 25 °C). The product is orange-flavored, distributed by Epic Pharma, LLC, with a net content of 378 g (168 g cholestyramine resin). The label also notes the product is from France and includes a blue section with the product name.*
FDA Label Image

Structure-formula.jpg (Structure Formula)

Structure-formula.jpg (Structure Formula)
Chemical structure of cholestyramine, depicting its polymeric form with benzene rings and quaternary ammonium groups as part of its repeating units, consistent with the active ingredient in CHOLESTYRAMINE 4 g/9 g powder for suspension by EPIC PHARMA, LLC.*

* 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.