Lactulose Solution
Product Images NDC 68999-002

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Lactulose (NDC 68999-002). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Chartwell Governmental & Specialty Rx, Llc., 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

FDA Label Image

"image Description" (Lactulose Oral Solution 15ml Unit Dose Label)

"image Description" (Lactulose Oral Solution 15ml Unit Dose Label)
Circular label for Lactulose Solution USP featuring 10 g/15 mL strength. The label states it delivers 15 mL per dose, includes the NDC number 68999-002-51, and is marked for institutional use only. It is manufactured by Chartwell Governmental & Specialty RX, LLC, with instructions not to freeze and to see the insert for more information.*
FDA Label Image

"image Description" (Lactulose Oral Solution 30ml Unit Dose Label)

"image Description" (Lactulose Oral Solution 30ml Unit Dose Label)
Round label for Lactulose Solution, USP 20 g/30 mL oral solution. The label includes the NDC 68999-004-43 and states "Delivers 30 mL." It is marked for institutional use only and manufactured for Chartwell Governmental & Specialty RX, LLC, Congers, NY. Additional instructions include "Do Not Freeze," with placeholders for lot number and expiration date.*
FDA Label Image

"image Description" (Lactulose Oral Solution Structure)

"image Description" (Lactulose Oral Solution Structure)
Chemical structure diagram of lactulose, illustrating its molecular arrangement with various hydroxyl groups and oxygen atoms in its saccharide rings.*

* 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.