Overview
Magnesium hydroxide is an inorganic compound. It is naturally found as the mineral brucite. Magnesium hydroxide can be used as an antacid or a laxative in either an oral liquid suspension or chewable tablet form. Additionally, magnesium hydroxide has smoke suppressing and flame retardant properties and is thus used commercially as a fire retardant. It can also be used topically as a deodorant or for the relief of canker sores (aphthous ulcers).
Indication
Magnesium hydroxide can be used as an antacid or a laxative depending on the administered dose. As an antacid, it is used for the temporary relief of heartburn, upset stomach, sour stomach or acid indigestion. As a laxative, it is used for the relief of occasional constipation by promoting bowel movements for 30 minutes and up to 6 hours.
Associated Conditions
- Colic
- Constipation
- Dyspepsia
- Flatulence
- Gastric Ulcer
- Heartburn
- Upset stomach
Clinical Trials
Title | Posted | Study ID | Phase | Status | Sponsor |
---|---|---|---|---|---|
2021/06/18 | N/A | Withdrawn | |||
2021/03/17 | Phase 2 | UNKNOWN | Dinara Zhumanbayeva | ||
2020/02/13 | Phase 1 | Completed |
FDA Drug Approvals
Approved Product | Manufacturer | NDC Code | Route | Strength | Effective Date |
---|---|---|---|---|---|
Geri-Care Pharmaceuticals, Corp | 57896-001 | ORAL | 1200 mg in 15 mL | 3/31/2025 | |
Kenvue Brands LLC | 16837-298 | ORAL | 165 mg in 1 1 | 8/7/2025 | |
H E B | 37808-121 | ORAL | 165 mg in 1 1 | 7/7/2025 | |
Cardinal Health 107, LLC | 55154-9429 | ORAL | 200 mg in 5 mL | 5/1/2025 | |
Preferred Pharmaceuticals Inc. | 68788-8638 | ORAL | 1200 mg in 15 mL | 8/12/2025 | |
Geri-Care Pharmaceuticals, Corp | 57896-004 | ORAL | 200 mg in 5 mL | 3/31/2025 | |
ATLANTIC BIOLOGICALS CORP. | 17856-0630 | ORAL | 200 mg in 5 mL | 5/12/2025 | |
Geri-Care Pharmaceuticals, Corp | 57896-002 | ORAL | 1200 mg in 15 mL | 3/31/2025 | |
ATLANTIC BIOLOGICALS CORP. | 17856-5725 | ORAL | 400 mg in 5 mL | 7/31/2025 | |
Contract Pharmacal Corp. | 10267-0041 | ORAL | 200 mg in 1 1 | 6/16/2025 |
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 |
---|---|---|---|---|---|
AXCEL EVILINE FORTE SUSPENSION | SIN06400P | SUSPENSION | 400 mg/5 ml | 7/4/1991 | |
HYDROSIL TABLET | SIN03484P | TABLET | 200 mg | 6/24/1989 | |
MACGEL TABLET | SIN08119P | TABLET | 200 mg | 4/11/1995 | |
ACTAL PLUS TABLET | SIN07376P | TABLET | 152 mg | 3/29/1993 | |
GASTROGEL ANTACID | SIN02976P | SUSPENSION | 24 mg/ml | 5/26/1989 | |
AXCEL EVILINE TABLET | SIN06592P | TABLET | 200 mg | 9/26/1991 |
NMPA Drug Approvals
Approved Product | Company | Approval Number | Drug Type | Dosage Form | Approval Date |
---|---|---|---|---|---|
No NMPA approvals found for this drug. |
PPB Drug Approvals
Approved Product | Registration No. | Company | Licence No. | Strength | Registration Date |
---|---|---|---|---|---|
VIDA-MECO SUSP ORAL | N/A | N/A | N/A | 2/6/1987 | |
SIMWELL CHEWABLE TABLETS | N/A | N/A | N/A | 11/6/2017 | |
GASEDIN-U EXTRA STOMACH CHEWABLE TAB | N/A | N/A | N/A | 12/28/2006 | |
MAALOX PLUS TAB | N/A | N/A | N/A | 10/12/1978 | |
FEDRA-GEL-S CHEWABLE TAB | N/A | N/A | N/A | 7/4/1984 | |
WEICHI TAB | N/A | N/A | N/A | 5/3/1995 |
TGA Drug Approvals
Approved Product | ARTG ID | Sponsor | Registration Type | Status | Registration Date |
---|---|---|---|---|---|
MYLANTA 2go ANTACID ORIGINAL chewable tablet (reformulation) blister pack | 118511 | Medicine | A | 5/11/2005 | |
GASTROGEL ANTACID oral liquid bottle | 13452 | Medicine | A | 8/30/1991 | |
MYLANTA DOUBLE STRENGTH oral liquid bottle (reformulation 2) | 126090 | Medicine | A | 3/10/2006 | |
MYLANTA ANTACID DOUBLE STRENGTH oral liquid bottle | 294406 | Medicine | A | 9/27/2017 | |
MYLANTA P ANTACID oral liquid bottle (reformulation) | 121994 | Medicine | A | 9/19/2005 | |
MYLANTA ORIGINAL oral liquid bottle (reformulation 2) | 122007 | Medicine | A | 9/19/2005 | |
MYLANTA ANTACID ORIGINAL oral liquid bottle | 294405 | Medicine | A | 9/27/2017 | |
Magnesia San Pellegrino Lemon Effervescent Powder | 10156 | Medicine | A | 6/24/1991 | |
MYLANTA P ANTACID chewable tablet blister pack | 118509 | Medicine | A | 5/11/2005 | |
MYLANTA 2go ANTACID DOUBLE STRENGTH chewable tablet (reformulation) blister pack | 118508 | Medicine | A | 5/11/2005 |
Health Canada Drug Approvals
Approved Product | Company | DIN | Dosage Form | Strength | Market Date |
---|---|---|---|---|---|
STOMAAX | theralab inc. | 00547239 | Suspension - Oral | 200 MG / 5 ML | 12/31/1982 |
GELUSIL EXTRA STRENGTH LIQ | warner-lambert canada inc. | 01945858 | Liquid - Oral | 350 MG / 5 ML | 12/31/1992 |
DIOVOL TABLETS | church & dwight canada corp | 00013838 | Tablet - Oral | 100 MG | 12/31/1968 |
PEPCID COMPLETE | mcneil consumer healthcare division of johnson & johnson inc | 02243053 | Tablet (Chewable) - Oral | 165 MG | 5/14/2001 |
ANTACID LIQUID SUSP | shoppers drug mart inc. | 00417920 | Suspension - Oral | 200 MG / 5 ML | 12/31/1977 |
ANTACID MAGNESIA AND ALUMINA | stanley pharmaceuticals, a division of vita health products inc. | 00854611 | Suspension - Oral | 200 MG / 5 ML | 12/31/1993 |
BABYS OWN TUMMY TAB | G.T. Fulford Pharmaceuticals | 00397083 | Tablet - Oral | 40 MG / TAB | 12/31/1977 |
MILK OF MAGNESIA-SUS 400MG/5ML | druggists' corporation | 02135914 | Suspension - Oral | 400 MG / 5 ML | 12/31/1995 |
GELUSIL ANTACID AND ANTI-GAS | 02409836 | Tablet (Chewable) - Oral | 200 MG | 1/14/2014 | |
MILK OF MAGNESIA MINERAL OIL EMULSION | bdh inc. | 02142996 | Emulsion - Oral | 6.4 % / 30 ML | 12/31/1995 |
CIMA AEMPS Drug Approvals
Approved Product | Company | Registration Number | Pharmaceutical Form | Prescription Type | Status |
---|---|---|---|---|---|
No CIMA AEMPS (Spain) approvals found for this drug. |
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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