FDA.reportPublic FDA data

Aluminum and Magnesium Hydroxide Suspension - Kesin Pharma Corporation

Manufacturer
Kesin Pharma Corporation
Effective date
2026-05-08
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 01:56:30

Label at a glance#

ProductKesin MAG-AL
Active ingredientALUMINUM HYDROXIDE, MAGNESIUM HYDROXIDE
Label structure11 sections

Indications and uses

For the relief of: acid indigestion heartburn sour stomach upset stomach due to these symptoms

Dosage and administration

shake well before using do not take more than 16 teaspoonfuls in 24 hours or use the maximum dosage for more than 2 weeks Age Dose adults and children 12 years of age and older take 2 to 4 teaspoonfuls four times a day or as directed by a physician children under 12 years of age consult a physician

Storage and handling

each teaspoonful (5 mL) contains: magnesium 200 mg, sodium < 1mg store at 20°C to 25°C (68°F to 77°F) Avoid freezing Alumag TM is a milky-white mint flavored suspension supplied in the following oral dosage forms: NDC 81033-005-30: 30 mL unit-dose cup NDC 81033-005-01: Case containing 100 unit-dose cups of 30 mL each.

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

OTC - ACTIVE INGREDIENT SECTION

OTC - PURPOSE SECTION

Active ingredient (in each 5 mL = 1 teaspoonful)………………….………..................................Purpose

Aluminum Hydroxide 200 mg……………………………………………………………………………..Antacid

Magnesium Hydroxide 200 mg…………………………………………………………………………...Antacid

Uses

INDICATIONS & USAGE SECTION

For the relief of:

  • acid indigestion
  • heartburn
  • sour stomach
  • upset stomach due to these symptoms

Warnings

WARNINGS SECTION

Do not take more than 16 teaspoonfuls in a 24-hour period or use the maximum dosage for more than 2 weeks except under the advice and supervision of a physician.

Ask a doctor before use if you have

OTC - ASK DOCTOR SECTION

  • kidney disease
  • a magnesium-restricted diet

Ask a doctor or pharmacist before use if you are

OTC - ASK DOCTOR/PHARMACIST SECTION

  • presently taking a prescription drug. Antacids may interact with certain prescription drugs.

Stop use and ask a doctor if

OTC - STOP USE SECTION

  • symptoms last more than 2 weeks

OTC - PREGNANCY OR BREAST FEEDING SECTION

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

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

  • shake well before using
  • do not take more than 16 teaspoonfuls in 24 hours or use the maximum dosage for more than 2 weeks
AgeDose
adults and children 12 years of age and oldertake 2 to 4 teaspoonfuls four times a day or as directed by a physician
children under 12 years of ageconsult a physician

Other information

STORAGE AND HANDLING SECTION

  • each teaspoonful (5 mL) contains: magnesium 200 mg, sodium < 1mg
  • store at 20°C to 25°C (68°F to 77°F)
  • Avoid freezing
  • Alumag TM is a milky-white mint flavored suspension supplied in the following oral dosage forms:

NDC 81033-005-30: 30 mL unit-dose cup
NDC 81033-005-01: Case containing 100 unit-dose cups of 30 mL each.

Inactive ingredients

INACTIVE INGREDIENT SECTION

colloidal silicon dioxide, glycerin, methylparaben, microcrystalline cellulose, mint flavor, propylene glycol, propylparaben, purified water, sorbitol, sucralose, xanthan gum

Questions or comments?

OTC - QUESTIONS SECTION

Call 1-833-537-4679

SPL UNCLASSIFIED SECTION

Distributed by:

Kesin Pharma

Oldsmar, FL 34677

PIS-005-V01

Rev. 10/2025

Kesin Pharma LogoKesin Pharma Logo

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC: 81033-005-01

Kesin MAG-AL TM 1200 mg/1200 mg per 30 mL

(Aluminum & Magnesium Hydroxide)

Delivers: 30 mL

Case = 100 UD Cups (Do Not Break Case)

Kesin MAG-AL Case LabelKesin MAG-AL Case Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC: 81033-005-01

Alumag TM 1200 mg/1200 mg per 30 mL (Aluminum & Magnesium Hydroxide)

Delivers: 30 mL

Case = 100 UD Cups (Do Not Break Case)

Alumag Case LabelAlumag Case Label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
243463aluminum hydroxide 200 MG / magnesium hydroxide 200 MG in 5 mL Oral SuspensionPSN2
243463aluminum hydroxide 40 MG/ML / magnesium hydroxide 40 MG/ML Oral SuspensionSCD2
243463aluminum hydroxide 1200 MG / magnesium hydroxide 1200 MG per 30 ML Oral SuspensionSY2
243463aluminum hydroxide 200 MG / milk of magnesia 200 MG per 5 ML Oral SuspensionSY2

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
Data codeCode 128K00000000Alumag_30mLCase_100ct.jpg, KesinMAG-ALTM_Case_30mL_100ct.jpg

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
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
c6b65c52-69c7-df49-550a-a50c137f6218Product name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
81033-005-01Kesin MAG-AL100 in 1 CASESUSPENSION1002
81033-005-30Kesin MAG-AL30 mL in 1 CUP, UNIT-DOSESUSPENSION302

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
81033-005-01ML - Milliliter81033-0059873b715-2772-4308-8cb1-dc8840090bfe12026-01-08
81033-005-30ML - Milliliter81033-0053cf538e4-dd95-4875-b15a-c6fa4a679b5212026-01-08

Products#

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

DailyMed product names page 1 of 1 · 17 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
81033-00581033-005-30, 81033-005-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 13 matching rows.

Name, UNII, Kind table
NameUNIIKind
SUCRALOSE96K6UQ3ZD4IACT
SILICON DIOXIDEETJ7Z6XBU4IACT
PROPYLPARABENZ8IX2SC1OHIACT
GLYCERINPDC6A3C0OXIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
SORBITOL506T60A25RIACT
MICROCRYSTALLINE CELLULOSEOP1R32D61UIACT
METHYLPARABENA2I8C7HI9TIACT
MINTFV98Z8GITPIACT
WATER059QF0KO0RIACT
ALUMINUM HYDROXIDE5QB0T2IUN0ACTIB
MAGNESIUM HYDROXIDENBZ3QY004SACTIB
XANTHAN GUMTTV12P4NEEIACT

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
12025-11-05monthly-update2026-06-03 17:39:53

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
Kesin MAG-ALALUMINUM AND MAGNESIUM HYDROXIDE SUSPENSIONKesin Pharma Corporation42df2198-14dc-da1c-e063-6394a90a1ae62026-05-08WarningsExact identifier
ndc (package): 81033-005-01
ndc (package): 81033-005-30
ndc (product): 81033-005
ndc11 (package): 81033000530
ndc11 (package): 81033000501
spl id: 515188f8-2cea-822a-e063-6394a90a3a2c
spl set id: 42df2198-14dc-da1c-e063-6394a90a1ae6

Reported adverse events (FAERS/openFDA)#

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