Lactulose Powder, For Solution
Product Images NDC 85592-819

Product Visual Gallery

This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Lactulose (NDC 85592-819). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Cumberland Assured Products 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

Structural Formula (Lac0c 0002 01)

Chemical structure of lactulose shown as two connected sugar rings with labeled atoms including carbon, oxygen, and hydrogen.*

FDA Label Image

Principal Display Panel (10 g Carton Label)

Packaging label for LACTULOSE Crystalline 10 grams powder for oral solution. The label indicates 30 single dose packets per container. The product is manufactured by Cumberland Assured Products Inc. The design features purple and white colors, with regulatory and dosing information noted, including an Rx only symbol.*

FDA Label Image

Principal Display Panel (10 g Pouch Label)

Label for LACTULOSE Crystalline powder for oral solution, 10 grams single dose packet. The label includes usage information, preparation directions to dissolve in 4 ounces of water, and manufacturer details: Cumberland Assured Products Inc., Nashville, TN. The label also displays the NDC 85592-819-01 and an Rx only symbol.*

FDA Label Image

Principal Display Panel (20 g Carton Label)

Label for LACTULOSE Crystalline 20 grams powder for oral solution by Cumberland Assured Products Inc. The carton indicates 30 single-dose packets, each containing 20 grams of crystalline lactulose. The label includes usage and preparation instructions, storage temperature, and Rx only designation.*

FDA Label Image

Principal Display Panel (20 g Pouch Label)

Label for LACTULOSE Crystalline 20 grams Powder for Oral Solution single dose packet. The label includes dosage information, preparation directions to dissolve the powder in water, and manufacturer details for Cumberland Assured Products Inc. The label also states that the unit dose packet is not child resistant and contains a barcode.*

* 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.