Lactulose Solution
Product Images NDC 0121-1154

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Lactulose (NDC 0121-1154). 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 diagram of lactulose, showing its molecular formula C12H22O11 with detailed depiction of the sugar rings and hydroxyl groups.*

FDA Label Image

Principal Display Panel (473 mL Bottle Label)

Label for Lactulose Solution USP 10 g/15 mL oral solution, manufactured by PAI Holdings, LLC dba PAI Pharma. The label includes storage instructions, product ingredients, dosing container size of 16 fl oz (473 mL), and directions for usual adult dosage. NDC 0121-0577-16 is shown along with a barcode and company information.*

FDA Label Image

Principal Display Panel (15 mL Cup Lid)

LACTULOSE Solution USP 10 g/15 mL unit dose label delivers 15 mL per unit. The label includes the NDC number 0121-4577-15, a barcode, and states the product is Rx only and the package is not child-resistant. The labeler is Pharmaceutical Associates, Inc., Greenville, SC.*

FDA Label Image

Principal Display Panel (30 mL Cup Lid)

LACTULOSE Solution USP 20 g/30 mL unit dose packaging label. The label is circular with a small tab for opening and includes dosage unit information, the NDC number 0121-1154-30, and a barcode. It is labeled as a prescription-only, non-child-resistant package, manufactured by Pharmaceutical Associates, Inc. in 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.