MAGNESIUM OXIDE, Magnesium Aluminum Hydrate

Manufacturer
Cho-A Pharm.Co.,Ltd.
Effective date
2017-02-28
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:49:01

Label at a glance#

ProductZantanol Tab.
Active ingredientMAGNESIUM OXIDE, MAGALDRATE
Label structure8 sections

Indications and uses

Helps relieve symptoms associated with indigestion: pain in the upper abdomen, heartburn, indigestion, nausea.

Dosage and administration

• do not take more than the recommended dose • adults (over 15 and under 80 years old): take 2 tablets per session. After 5 hours if symptoms last 0.5-1g per session, 1-3 times per day, before meal. Do not take over 4 tablets a day.

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Magnesium Aluminum Hydrate 100mg

Magnesium Oxide 50mg

Purpose

OTC - PURPOSE SECTION

Antacid

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

• In case of overdose, get medical help or contact a Poison Control Center (1-800-222-1222) right away.

Uses

INDICATIONS & USAGE SECTION

Helps relieve symptoms associated with indigestion: pain in the upper abdomen, heartburn, indigestion, nausea.

Warnings

WARNINGS SECTION

For oral use only

Use only the recommended dosage

Do not use if you have
• hemodyscrasia
• kidney, liver, bowel, stomach, and duodenum disease
• immunological disorder (asthma,rheumatism)
• previously experienced sensitivity to this medication
• dialysis

Do not use if the user under 15 and over 80 years old.

When using this product
• do not take other stomach medicine.
• do not take alcohol

Ask a doctor, dentist, or pharmacist before use if the user
• take other medication
• take medical treatment
• have allergic reaction for drug
• are over 65 years old
• have sore throat, cough, or fever
• are having continuously stomachaches
• have kidney disease

If pregnant or breast-feeding, ask a health professional before use.

Store at cool temperature and dry place with a closed container. Avoid direct sunlight. - Store in a container other than its original container is equivalent to misuse. In order to prevent the reduction of drug efficacy, keep the product in its original container for storage.

Directions

DOSAGE & ADMINISTRATION SECTION

• do not take more than the recommended dose
• adults (over 15 and under 80 years old): take 2 tablets per session. After 5 hours if symptoms last 0.5-1g per session, 1-3 times per day, before meal. Do not take over 4 tablets a day.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Ranitidine Hydrochloride, Magnesium Aluminosilicate, Low Substituted Hydroxypropylcellulose, Crospovidone, Hydroxypropylcellulose, Magnesium Stearate, Opadry white 80W68912, Purified Water

Zantanol Tab.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

zantanolzantanol

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
MAGNESIUM CATION Pharmacologic Class Indexing4Indexing - Pharmacologic Class20180813

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
6e3c022f-0786-43f1-8857-edff89d5153fProduct name120260309
95250459-30e4-45c1-b08a-993044f49109Product name220250805
efd58652-cb8f-4018-91ca-4b0eb2ff729fProduct name720240226
362d7abb-94e6-4c60-9a58-266894157713Product name120231023
e2db08c6-133f-4f4f-afb4-e90a2418d6f6Product name120230320
6bd95106-a412-1dad-b9cc-4cb74bfb27ceProduct name220230315
9badc7be-250a-44ab-aa36-926af3f02679Product name120210527
2641ccb3-721d-4fbf-9f2f-ca2f18157a62Product name320210309
7f54af34-be54-4c3c-894f-78df6452d747Product name320190703
ccf8541e-b7dc-e6ba-06c9-15bf143a7850Product name520190611
11ed6f83-cdd2-4637-8379-b1a1d3ae3cdeProduct name120181101
05700d9e-ea6f-4aab-b0ed-1488f1d85d7bProduct name120180904
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
86c45a79-b9f0-4476-a27c-6e10db098497Product name120180125
26acd337-b838-40ac-bcbc-05c3b81c8712Product name120170323
2f9d4e5c-e179-490e-8c43-f19e1e0ca228Product name120160720
d5e51f11-ad28-caa4-4b49-4143974782adProduct name120150831
290f523a-f9db-9774-b5a9-e1f908ac1782Product name120150828
e7e58cd3-cacb-49df-8d34-1ee335614abbProduct name120150609
0ca1d589-929b-4b33-bc5b-1d84abdafa6aProduct name120150324
fc363c46-397b-4476-ac0f-70e43e8e4592Product name120150324
c6b65c52-69c7-df49-550a-a50c137f6218Product name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
58354-101-022020-01-31C16284748780-19d75b9d1-04b3-f424-e053-dadaa90a57ceZantanol Tab.

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
58354-101-01Zantanol Tab.424 mg in 1 CAPSULETABLET4241
58354-101-02Zantanol Tab.10 in 1 PACKAGETABLET101

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
58354-101ZANTANOL TAB. (MAGNESIUM OXIDE, MAGNESIUM ALUMINUM HYDRATE) TABLET [CHO-A PHARM.CO.,LTD.]1Legacy NDC, 2 package rows20170301_9b3092fa-86e6-469d-8f73-0626e4c12a28.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 13 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
58354-10158354-101-01, 58354-101-02

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 9 matching rows.

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
bcdeaf1a-6dcd-4ebe-b50a-b4bc91aa418f9b3092fa-86e6-469d-8f73-0626e4c12a282017-02-28WarningsExact identifier
spl id: bcdeaf1a-6dcd-4ebe-b50a-b4bc91aa418f
spl set id: 9b3092fa-86e6-469d-8f73-0626e4c12a28

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.