Lactulose Solution
Product Images NDC 0121-0873

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Lactulose (NDC 0121-0873). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Pai Holdings, Llc Dba Pai Pharma, 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

Chemical Structure (Lactulose 01)

Chemical structure of lactulose, showing its molecular composition and arrangement, with the molecular formula C12H22O11 depicted.*

FDA Label Image

Principal Display Panel (473 mL Bottle Label)

Label for Lactulose Solution USP 10 g/15 mL oral solution by PAI Holdings, LLC dba PAI Pharma. Contains product strength, dosage form, 16 fl oz (473 mL) bottle size, storage instructions at 20° to 25°C, and pharmacist ordering notes. The label includes directions for usual adult dosage and storage warnings.*

FDA Label Image

Principal Display Panel (15 mL Cup Lid)

Label of LACTULOSE solution USP 10 g/15 mL unit dose vial by Pharmaceutical Associates, Inc. The label indicates a 15 mL unit dose and states it is not child-resistant. It includes an NDC code 0121-0873-15 and notes the product is for prescription use only.*

FDA Label Image

Principal Display Panel (30 mL Cup Lid)

LACTULOSE Solution USP 20 g/30 mL unit dose label. The label states it delivers 30 mL per unit dose and is indicated for the treatment of constipation, referencing the insert for details. It includes the NDC 0121-1746-30 and states Rx Only. The labeler is Pharmaceutical Associates, Inc., Greenville, SC.*

* 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.