Product Images Lactulose

View Photos of Packaging, Labels & Appearance

Product Label Images

The following 4 images provide visual information about the product associated with Lactulose NDC 0121-4577 by Pai Holdings, Llc, such as packaging, labeling, and the appearance of the drug itself. This resource could be helpful for medical professionals, pharmacists, and patients seeking to verify medication information and ensure they have the correct product.

Chemical Structure - lactulose 01

Chemical Structure - lactulose 01

PRINCIPAL DISPLAY PANEL - 473 mL Bottle Label - lactulose 02

PRINCIPAL DISPLAY PANEL - 473 mL Bottle Label - lactulose 02

This is a description for a medication called lactulose solution. It is recommended to be stored at a controlled room temperature between 20°C to 25°C (68°F to 77°F) and not frozen. The therapeutic action is not affected by slight darkening of the product. The medication is not to be used if there is extreme darkening or turbidity, and the packaging has instructions for use. Each 15mL contains 10g of lactulose along with other ingredients like purified water, FD&C Yellow No.6, and flavoring. The recommended adult dosage is between 15mL to 30mL daily, and the medication is used to treat constipation.*

PRINCIPAL DISPLAY PANEL - 15 mL Cup Lid - lactulose 03

PRINCIPAL DISPLAY PANEL - 15 mL Cup Lid - lactulose 03

This is a unit dose of Lactulose solution USP 10g/15mL, indicated for the treatment of constipation. The package is not child-resistant and should only be used under prescription. The NDC code is 0121-4577-15, and it is produced by Pharmaceutical Associates, Inc. located in Greenville, South Carolina. For more information about usage, refer to the insert.*

PRINCIPAL DISPLAY PANEL - 30 mL Cup Lid - NDC 0121-1154-30 - lactulose 04

PRINCIPAL DISPLAY PANEL - 30 mL Cup Lid - NDC 0121-1154-30 - lactulose 04

This is a description of a pharmaceutical product. It is a Lactulose solution (20 g/30 mL) indicated for the treatment of constipation. The product is packaged in single-unit doses that deliver 30 mL of solution. The national drug code (NDC) for this product is 0121-1154-30. The package is labeled as Rx-only and has a warning that it is not child-resistant. The manufacturer of the product is Pharmaceutical Associates, Inc. based in Greenville, SC 29605.*

* The product label images have been analyzed using a combination of traditional computing and machine learning techniques. It should be noted that the descriptions provided may not be entirely accurate as they are experimental in nature. Use the information in this page at your own discretion and risk.