Kristalose Powder, For Solution
Product Images NDC 66220-729
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Product Visual Gallery
This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Kristalose (NDC 66220-729). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.
As provided by Cumberland 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.
Product Images & Figures Index
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Kristalose® is a lactulose-based oral solution used for treating constipation. The usual adult dosage is 10-20 grams daily, dissolved in half a glass of water. Since lactulose takes time to reach the colon, it may take 24-48 hours for a normal bowel movement to occur. The solution is contained in a single-use packet, which is not resistant to children. Each packet contains 10 grams of lactulose, with less than 0.3 g galactose and lactose combined. The solution should be stored at room temperature (15°-30°C). Kristalose is manufactured by Cumberland Pharmaceuticals Inc. *
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This is a product description for lactulose, an oral solution for treating constipation. Each packet contains 20 grams of lactulose and less than 0.6 g of galactose and lactose as a total sum. The packet is not child-resistant. An accompanying package insert provides information on indications and dosage instructions, with the usual adult dosage being 10 to 20 grams a day. Lactulose can take 24-48 hours to produce a bowel movement. The product is to be dissolved in half a glass of water and stored at room temperature. It is manufactured by Cumberland Pharmaceuticals Inc. based in Nashville, TN, USA.*
* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.