MAALOX

This brand name is authorized in Austria, Cyprus, Estonia, France, Ireland, Israel, Japan, Lithuania, Malta, Netherlands, Poland, South Africa, UK.

Active ingredients

The drug MAALOX contains a combination of these active pharmaceutical ingredients (APIs):

1
UNII LMI26O6933 - ALUMINUM OXIDE
 

Aluminium hydroxide is a slow-acting antacid. It is used to provide symptomatic relief in gastric hyperacidity. In addition, the antipeptic and demulcent activity of aluminium hydroxide helps to protect inflamed gastric mucosa against further irritation by gastric secretions.

 
Read more about Aluminium hydroxide
2
UNII NBZ3QY004S - MAGNESIUM HYDROXIDE
 

Magnesium hydroxide is practically insoluble in water and solution is not effected until the hydroxide reacts with hydrochloric acid in the stomach to form magnesium chloride. Its neutralising action is almost equal to that of sodium bicarbonate. When the dose is in excess of that required to neutralise the acid the intragastric pH may reach pH 8 or 9. Acid rebound following magnesium hydroxide is clinically insignificant. Magnesium hydroxide has an indirect cathartic effect resulting from water retention in the intestinal lumen.

 
Read more about Magnesium hydroxide

Medication package inserts

Below package inserts are available for further reading:

Document Type Information Source  
 MAALOX Oral suspension MPI, EU: SmPC Health Products Regulatory Authority (IE)

Medicine classification

This drug has been classified in the anatomical therapeutic chemical (ATC) classification system as follows:

ATC Group Classification
A02AA04 Magnesium hydroxide A Alimentary tract and metabolism → A02 Drugs for acid related disorders → A02A Antacids → A02AA Magnesium compounds
Discover more medicines within A02AA04
A02AB01 Aluminium hydroxide A Alimentary tract and metabolism → A02 Drugs for acid related disorders → A02A Antacids → A02AB Aluminium compounds
Discover more medicines within A02AB01
A02AB10 Combinations A Alimentary tract and metabolism → A02 Drugs for acid related disorders → A02A Antacids → A02AB Aluminium compounds
Discover more medicines within A02AB10
A02AD01 Ordinary salt combinations A Alimentary tract and metabolism → A02 Drugs for acid related disorders → A02A Antacids → A02AD Combinations and complexes of aluminium, calcium and magnesium compounds
Discover more medicines within A02AD01

Authorization and marketing

This drug has been assigned below unique identifiers within the countries it is being marketed:

Country Identification scheme Identifier(s)
EE Ravimiamet 1009167, 1390531, 1390632, 1390643, 1645028, 1645039
FR Base de données publique des médicaments 60330700, 62245483, 64216427, 67189387, 69221111, 69545939
GB Medicines & Healthcare Products Regulatory Agency 347155
IL מִשְׂרַד הַבְּרִיאוּת 1307
JP 医薬品医療機器総合機構 2349101D1253
LT Valstybinė vaistų kontrolės tarnyba 1006908, 1006909, 1035290, 1035398, 1055196
MT Medicines Authority AA1470/01401
PL Rejestru Produktów Leczniczych 100082325, 100082331, 100291030
ZA Health Products Regulatory Authority 42/11.4.1/0390, E/11.4.1/1271, E/11.4.1/1272

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