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Magnesium trisilicate

Generic Name
Magnesium trisilicate
Brand Names
Gaviscon Chewable
Drug Type
Small Molecule
Chemical Formula
Mg2O8Si3
CAS Number
14987-04-3
Unique Ingredient Identifier
FML8G1U0Y3

Overview

Magnesium trisilicate is an inorganic compound that is used as an antacid in the treatment of peptic ulcers.

Indication

For the treatment of peptic ulcers. Relieving indigestion and heartburn.

Associated Conditions

  • Bloating
  • Colic
  • Dyspepsia
  • Flatulence
  • Gastric Ulcer
  • Heartburn
  • Reflux Acid
  • Upset stomach

Clinical Trials

Title
Posted
Study ID
Phase
Status
Sponsor

No clinical trials found

No clinical trials found for this drug

FDA Drug Approvals

Approved Product
Manufacturer
NDC Code
Route
Strength
Effective Date
Haleon US Holdings LLC
0135-0096
ORAL
14.2 mg in 1 1
5/15/2025

EMA Drug Approvals

Approved Product
Authorization Holder
Status
Issued Date
No EMA approvals found for this drug.

HSA Drug Approvals

Approved Product
Manufacturer
Approval Number
Dosage Form
Strength
Approval Date
MAGNESIUM TRISILICATE COMPOUND TABLET BP
SIN06599P
TABLET
250 mg
10/1/1991
MAGTASIL ANTACID MIXTURE
SIN08786P
SUSPENSION
5% w/v
7/3/1996
ALLUMAG MPS TABLET
SIN09497P
TABLET
100 mg
9/22/1997
SEMOR STOMACH TABLET
SIN03314P
TABLET
250 mg
6/8/1989
GUARDIAN ANTACID TABLET
SIN08171P
TABLET
250 mg
5/12/1995
WELUSIL TABLET
SIN05336P
TABLET
250mg
1/12/1991
ALUMAG PLUS TABLETS
SIN03547P
TABLET
250 mg
6/6/1989
SUNTACID TABLET
SIN07066P
TABLET
250 mg
6/18/1992
POLYSILIC III SUSPENSION
SIN03406P
SUSPENSION
400 mg/5 ml
6/16/1989
ALLUMAG M TABLET
SIN09499P
TABLET
250 mg
9/25/1997

NMPA Drug Approvals

Approved Product
Company
Approval Number
Drug Type
Dosage Form
Approval Date
No NMPA approvals found for this drug.

TGA Drug Approvals

Approved Product
ARTG ID
Sponsor
Registration Type
Status
Registration Date
QUICK-EZE tablet chewable wrapping
97501
Medicine
A
10/9/2003
GASTROGEL ANTACID oral liquid bottle
13452
Medicine
A
8/30/1991
QUICK-EZE TABLET CHEWABLE blister pack
191398
Medicine
A
11/2/2011
QUICK-EZE TABLET CHEWABLE wrapping reformulated
189816
Medicine
A
9/23/2011

Health Canada Drug Approvals

Approved Product
Company
DIN
Dosage Form
Strength
Market Date
R90 ANTI-ACIDE TAB
dr reckeweg canada
02001004
Tablet - Oral
500 MG / TAB
12/31/1993
GASULSOL TAB
herbes universelles inc.
00361704
Tablet - Oral
130 MG
12/31/1966
ALKA PHENYL TAB
00430900
Tablet - Oral
150 MG / TAB
12/31/1978
SPASMO NIL TAB
00430897
Tablet - Oral
75 MG
12/31/1978
GASVA
les produits gerbex inc.
00109797
Tablet - Oral
487.5 MG / TAB
12/31/1970
PHENYLONE PLUS TAB
medic laboratory ltée
00432954
Tablet - Oral
150 MG / TAB
12/31/1978
ALKA PHENYLBUTAZONE TAB
PRO DOC LIMITEE
00291854
Tablet - Oral
150 MG / TAB
12/31/1974
GASTROCOTE CHEWABLE TAB
stanley pharmaceuticals, a division of vita health products inc.
01941879
Tablet - Oral
40 MG
12/31/1992
COMPOSE 511 TAB
alimentex inc.
00495328
Tablet - Oral
120 MG / TAB
12/31/1979
MAG-A-FOLIC TAB
00748250
Tablet - Oral
100 MG / TAB
12/31/1989

CIMA AEMPS Drug Approvals

Approved Product
Company
Registration Number
Pharmaceutical Form
Prescription Type
Status
MIRPEDIL COMPRIMIDOS MASTICABLES
Angelini Pharma Espana S.L.
49935
COMPRIMIDO
Sin Receta
Not Commercialized
SECREPAT COMPRIMIDOS MASTICABLES SABOR ANIS
Angelini Pharma Espana S.L.
83167
COMPRIMIDO MASTICABLE
Sin Receta
Not Commercialized
SECREPAT COMPRIMIDOS MASTICABLES SABOR MENTA
Angelini Pharma Espana S.L.
80048
COMPRIMIDO MASTICABLE
Sin Receta
Not Commercialized
GELODROX SUSPENSION ORAL
32243
SUSPENSIÓN ORAL
Sin Receta
Not Commercialized

Philippines FDA Drug Approvals

Approved Product
Company
License Number
Dosage Form
Strength
Approval Date
No Philippines FDA approvals found for this drug.

Saudi SFDA Drug Approvals

Approved Product
Company
License Number
Dosage Form
Strength
Approval Date
No Saudi SFDA approvals found for this drug.

Malaysia NPRA Drug Approvals

Approved Product
Company
Registration Number
Dosage Form
Strength
Approval Date
No Malaysia NPRA approvals found for this drug.

UK EMC Drug Information

Medicine Name
MA Holder
MA Number
Pharmaceutical Form
Active Ingredient
Authorization Date
No UK EMC drug information found for this drug.

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