Lactulose Solution
Product Images NDC 0121-0873
View Photos of Packaging, Regulatory Labels, and Product Appearance
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.
Principal Display Panel (473 mL Bottle Label)
This is a description for a lactulose solution used for treating constipation. It contains 10g of lactulose in 15mL and should be stored at room temperature between 20-25°C. It should not be frozen as it may darken slightly but its therapeutic action is not affected. The product should not be used if extreme darkening or turbidity occurs. The usual adult dosage is 1-2 tablespoonfuls (15 to 30 mL) daily, as per the accompanying product information. It is important to keep the product tightly closed in the original container or a light-resistant container with a child-resistant closure. The product number or NDC should be included while ordering the product.*
Principal Display Panel (15 mL Cup Lid)
This is a unit dose label for lactulose solution USP with a concentration of 10 g/15 mL. The medication is used to treat constipation. It is produced and distributed by Pharmaceutical Associates Inc. It is a prescription-only medication and should be kept out of reach of children. The label includes information on dosage (15 mL per dose) and product identification (NNDC 0121-0873-15).*
Principal Display Panel (30 mL Cup Lid)
This is a product labeled as LACTULOSE with a package size of 30mL. It is intended for the treatment of constipation, and the manufacturer is PPHARMACEUTICAL ASSOCIATES, located in Greenville, SC. The product is not child-resistant, and the instruction for use is available in the insert that comes with the product. The National Drug Code (NDC) assigned to this product is 0121-1746-30.*
* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.