Active ingredient: 670 grams of bovine lactulose in 1000 mL aqueous solution

Excipients: ORALAC does not contain any excipients, but may contain small amounts of sugars (e.g. bovine lactose, galactose, epilactose, fructose) and sulphite residues from the production route, which have known effects.

Before you start using this medicine, read this INSTRUCTIONS FOR USE carefully, because it contains important information for you.

ORALAC is a clear, colorless or pale brown-yellow, viscous solution for oral use. It is presented in high density polyethylene bottles with a measuring cup.

ORALAC contains a laxative called lactulose. Lactulose softens the stool (stool) by drawing water into the intestine and facilitates its passage through the intestine. Lactulose is not absorbed by your body.

It is used to treat the following conditions:

Instructions for proper use and dosage/frequency of administration

Always use ORALAC as directed by your doctor or pharmacist. If you are not sure, consult your doctor or pharmacist.

Dosing in cases of constipation or when the stool consistency is medically desired to be soft

ORALAC can be taken as a single daily dose or divided into two doses.

Dosing in Hepatic Encephalopathy (adults only)

Like all medicines, ORALAC may have side effects in people who are sensitive to its ingredients.

The frequency of observed side effects is described as follows:

If any of the following occur, stop using ORALAC and IMMEDIATELY inform your doctor or go to the emergency department of your nearest hospital:

These are all very serious side effects.

If you have one of these, it means you have a serious allergy to ORALAC.

⚠️ Disclaimer: The information provided on this website is for informational purposes only and does not substitute professional medical advice. Always consult a healthcare provider before using any medication.