MAGNESIUM HYDROXIDE

Manufacturer
Shandong Zhouyu Fire Technology Co.,Ltd
Effective date
2023-09-08
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:56:08

Label at a glance#

ProductMAGNESIUM HYDROXIDE
Active ingredientMAGNESIUM HYDROXIDE, CALCIUM CHLORIDE
Label structure11 sections

Indications and uses

For stomach upset , oral problems , skin fungi andstaphylococcus aureus , candida albicans , E coli andother problems , to neutralize the body's acid base andprovide relief , supplement magnesium and so on. Used to supplement calcium and regulateelectrolyte balance , treat calcium deficiency and someelectrolyte imbalance

Storage and handling

Store in a cool and dry place , if the product is stored ina cold place , it may cause the product to be cloudythe efficacy is unchanged , safe and reliable

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Magnesium hydroxide 14%

calcium chloride 0.001%

OTC - PURPOSE SECTION

For stomach upset , oral problems , skin fungi and staphylococcus aureus , candida albicans , E coli andother problems , to neutralize the body's acid base and provide relief , supplement magnesium and so on.

Used to supplement calcium and regulate electrolyte balance , treat calcium deficiency and some electrolyte imbalance

Uses

INDICATIONS & USAGE SECTION

For stomach upset , oral problems , skin fungi andstaphylococcus aureus , candida albicans , E coli andother problems , to neutralize the body's acid base andprovide relief , supplement magnesium and so on.

Used to supplement calcium and regulateelectrolyte balance , treat calcium deficiency and someelectrolyte imbalance

OTC - DO NOT USE SECTION

If you accidentally enter the eyes during use , rinse immediately with water . Keep away from children . In case of adverse reactions , stop using immediately and seek medical attention . Do not use this product if you have an allergic reaction to the relevant ingredients

OTC - WHEN USING SECTION

It is recommended to dilute 50 times , 3-5 times a day ,and adjust according to personal circumstances

OTC - STOP USE SECTION

If you accidentally enter the eyes during use , rinse immediately with water . Keep away from children . In case of adverse reactions , stop using immediately and seek medical attention . Do not use this product if you have an allergic reaction to the relevant ingredients

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep away from children

DOSAGE & ADMINISTRATION SECTION

It is recommended to dilute 50 times , 3-5 times a day ,and adjust according to personal circumstances

Storage conditions

STORAGE AND HANDLING SECTION

Store in a cool and dry place , if the product is stored ina cold place , it may cause the product to be cloudythe efficacy is unchanged , safe and reliable

inactive ingredient

INACTIVE INGREDIENT SECTION

water

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

83674-001-0183674-001-01

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
CALCIUM CATION Pharmacologic Class Indexing3Indexing - Pharmacologic Class20230427

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
6e3c022f-0786-43f1-8857-edff89d5153fProduct name120260309
95250459-30e4-45c1-b08a-993044f49109Product name220250805
bee4fa8d-8d82-423a-a0b5-40a89dd13a99Product name120250618
e0d2eb29-08bd-4bba-90d1-c91c68a38767Product name420250516
30b0ac6e-02aa-0e5c-0d8b-cffdf3a282b2Product name520250304
334fe8d2-68fb-4331-a576-420e302ec069Product name720240320
efd58652-cb8f-4018-91ca-4b0eb2ff729fProduct name720240226
362d7abb-94e6-4c60-9a58-266894157713Product name120231023
e2db08c6-133f-4f4f-afb4-e90a2418d6f6Product name120230320
6bd95106-a412-1dad-b9cc-4cb74bfb27ceProduct name220230315
3c386306-c48a-413e-bb69-70cb268496f3Product name120210727
9badc7be-250a-44ab-aa36-926af3f02679Product name120210527
2641ccb3-721d-4fbf-9f2f-ca2f18157a62Product name320210309
444b3e50-f226-46ef-bfca-2e7035d140cdProduct name120190611
e92765c1-be81-432a-b909-1b10777ec378Product name120190208
11ed6f83-cdd2-4637-8379-b1a1d3ae3cdeProduct name120181101
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
86c45a79-b9f0-4476-a27c-6e10db098497Product name120180125
26acd337-b838-40ac-bcbc-05c3b81c8712Product name120170323
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
0441a8f5-3835-497c-aedd-bc78cba56b2aProduct name120150317
87711080-88eb-65c5-b2dd-bf99e700a372Product name120140508
c6b65c52-69c7-df49-550a-a50c137f6218Product name120140508
ec2149b3-5c6d-5344-f757-c86411073075Product name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
83674-001-012024-07-30C16284748780-11030e365-152f-111a-e063-dadaa90a10e204e3e713-4d0a-fffd-e063-6394a90a4f95
83674-001-012024-01-30C16284748780-11030e365-152f-111a-e063-dadaa90a10e204e3e713-4d0a-fffd-e063-6394a90a4f95

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
83674-001-01MAGNESIUM HYDROXIDE50 in 1 BOXLIQUID501
83674-001-02MAGNESIUM HYDROXIDE5 g in 1 BOTTLELIQUID51

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
83674-001MAGNESIUM HYDROXIDE LIQUID [SHANDONG ZHOUYU FIRE TECHNOLOGY CO.,LTD]12 package rows20230910_04e3e713-4d0a-fffd-e063-6394a90a4f95.zip

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
83674-00183674-001-02, 83674-001-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
MAGNESIUM HYDROXIDENBZ3QY004SACTIB
CALCIUM CHLORIDEM4I0D6VV5MACTIB

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
04e3e713-4d0b-fffd-e063-6394a90a4f9504e3e713-4d0a-fffd-e063-6394a90a4f952023-09-08Exact identifier
spl id: 04e3e713-4d0b-fffd-e063-6394a90a4f95
spl set id: 04e3e713-4d0a-fffd-e063-6394a90a4f95

Reported adverse events (FAERS/openFDA)#

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