Formula (F2fc77b5 4ac9 469a B2c2 4ba2c8b05a3b 01)
Cholestyramine Powder, For Suspension
Product Images NDC 70771-1070
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Product Visual Gallery
This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Cholestyramine (NDC 70771-1070). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.
As provided by Zydus Lifesciences Limited, these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.
Label (F2fc77b5 4ac9 469a B2c2 4ba2c8b05a3b 02)
This is a set of instructions for preparing Cholestyramine for Oral Suspension USP Light Powder. It includes information on measuring, mixing, and adding water. It is important to mix the powder with a noncarbonated beverage or water before consuming. It contains phenylalanine and should be kept out of the reach of children. The usual dosage must be verified by the enclosed literature. The container should be tightly closed after use. The product is flavored with orange and vanilla.*
Carton (F2fc77b5 4ac9 469a B2c2 4ba2c8b05a3b 03)
This text provides instructions for the preparation of Cholestyramine oral suspension USP light powder, which can be mixed with highly fluid foods, fruits or non-carbonated beverages. It gives instructions on how to mix one or more pouches of the product and includes a note on the use of NutraSweet sweetener. The text also includes product information such as packaging details and the grams of cholestyramine resin per pouch.*
* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.
