Home NDC 81033-005 Kesin MAG-AL
Product NDC 81033-005
11-digit product format 810330005
Labeler code 81033
Product ID 81033-005_515188f8-2cea-822a-e063-6394a90a3a2c
Type HUMAN OTC DRUG
Nonproprietary name Aluminum and Magnesium Hydroxide Suspension
Dosage form SUSPENSION
Route ORAL
Labeler Kesin Pharma Corporation
Application M001
Marketing category OTC MONOGRAPH DRUG
Marketing start 2025-11-05
Substance ALUMINUM HYDROXIDE; MAGNESIUM HYDROXIDE
Active strength 200; 200 mg/5mL; mg/5mL
Pharmacologic classes Calculi Dissolution Agent [EPC], Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Inhibition Small Intestine Fluid/Electrolyte Absorption [PE], Magnesium Ion Exchange Activity [MoA], Osmotic Activity [MoA], Osmotic Laxative [EPC], Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]
NDC exclude flag No
Listing certified through 2027-12-31
Current FDA listing Yes Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base Kesin MAG-AL
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ALUMINUM HYDROXIDE 200 mg/5mL MAGNESIUM HYDROXIDE 200 mg/5mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 5QB0T2IUN0 Internal UNII lookup NBZ3QY004S Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 243463 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 81033-005-01 Kesin MAG-AL 100 in 1 CASE SUSPENSION 100 2 81033-005-30 Kesin MAG-AL 30 mL in 1 CUP, UNIT-DOSE SUSPENSION 30 2
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 17 of 34 · 678 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Ultra Strength CALCIUM CARBONATE BETTER LIVING BRANDS LLC 3ff92c9a-987f-468e-9e18-1e3e171ede14 2025-10-29 Warnings Exact identifier application number: M001 Ultra Strength CALCIUM CARBONATE BETTER LIVING BRANDS LLC 35b3d9d0-b04d-4f6d-b99d-435233803d4b 2025-10-29 Warnings Exact identifier application number: M001 Ultra Strength ANTACID TABLETS SAFEWAY 4c6cdd81-5145-4a1f-888f-85cf5d856c39 2025-10-29 Warnings Exact identifier application number: M001 Extra Strength Smooth ANTACID TABLETS SAFEWAY 8ed35c3b-9878-4889-90f7-a3973cf806e0 2025-10-29 Warnings Exact identifier application number: M001 Publix Regular Strength Assorted Fruit CALCIUM CARBONATE PUBLIX SUPER MARKETS, INC fd637431-7a08-4454-9cae-a68716d2d0fa 2025-10-28 Warnings Exact identifier application number: M001 Publix Regular Strength Peppermint Flavor CALCIUM CARBONATE PUBLIX SUPER MARKETS, INC c41b6cc2-c852-45fd-858c-c7bedc5dc882 2025-10-28 Warnings Exact identifier application number: M001 Publix Extra Strength Assorted Berry CALCIUM CARBONATE PUBLIX SUPER MARKETS, INC a270fc36-f2b2-4f56-81d4-cf165f6b5abe 2025-10-28 Warnings Exact identifier application number: M001 Extra Strength Sugar Free Orange Cream Flavor CALCIUM CARBONATE PUBLIX SUPER MARKETS, INC 4dbdabc4-280d-4c9a-8c54-84afc615c8c7 2025-10-28 Warnings Exact identifier application number: M001 Publix Extra Strength Tropical Fruit CALCIUM CARBONATE PUBLIX SUPER MARKETS, INC 28e8dd03-25cf-43db-8c4d-3aae99be9d53 2025-10-28 Warnings Exact identifier application number: M001 Publix Ultra Strength Assorted Fruit CALCIUM CARBONATE PUBLIX SUPER MARKETS, INC 9e1c883f-016e-4c05-b27a-750d14c0f3e5 2025-10-28 Warnings Exact identifier application number: M001 Ultra Strength Antacid CALCIUM CARBONATE Wal-Mart Stores,Inc., 48827658-02f7-4599-a90a-1543b30b9de1 2025-10-27 Warnings Exact identifier application number: M001 Regular Strength Antacid ANTACID Wal-Mart Stores,Inc., 6e7cd170-b169-4fc0-bc90-f4421bbd9fcd 2025-10-27 Warnings Exact identifier application number: M001 equate Extra Strength Antacid CALCIUM CARBONATE Wal-Mart Stores,Inc., febe9d70-9a1f-43a9-8ad0-3134eefc6967 2025-10-27 Warnings Exact identifier application number: M001 equate Extra Strength Antacid CALCIUM CARBONATE Wal-Mart Stores,Inc., d399f927-e80b-4162-a1f1-ef6159d6f7b1 2025-10-27 Warnings Exact identifier application number: M001 equate Sugar Free Extra Strength Antacid Orange Cream Flavor ANTACID Wal-Mart Stores,Inc., 53a22b37-66af-4735-b262-15e06ad7bf76 2025-10-27 Warnings Exact identifier application number: M001 equate Extra Strength Antacid CALCIUM CARBONATE Wal-Mart Stores,Inc. 841ddf88-a016-4a3c-9508-5d5702883d8f 2025-10-27 Warnings Exact identifier application number: M001 Ultra Strength Antacid Assorted Fruit CALCIUM CARBONATE Wal-Mart Stores,Inc., 6900fabc-2299-48cf-bbda-c92649cfd0e1 2025-10-27 Warnings Exact identifier application number: M001 equate Ultra Strength Antacid Peppermint Flavor ANTACID TABLETS Wal-Mart Stores,Inc., 6a18cd92-cc51-401b-9074-fbaa1afb42ac 2025-10-27 Warnings Exact identifier application number: M001 Extra Strength Smooth Antacid ANTACID TABLETS Wal-Mart Stores,Inc., 9acdfb08-043d-48a5-95f9-54bcba733c6e 2025-10-27 Warnings Exact identifier application number: M001 equate Extra Strength Antacid ALUMINUM HYDROXIDE AND MAGNESIUM CARBONATE Wal-Mart Stores,Inc 448d1c72-2308-4041-8ba6-dd1e0802cc47 2025-10-27 Warnings Exact identifier application number: M001
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 81033-005-01 81033000501 100 CUP, UNIT-DOSE in 1 CASE (81033-005-01) / 30 mL in 1 CUP, UNIT-DOSE (81033-005-30) 2025-11-05 No No Current 81033-005-30 81033000530 30 mL in 1 CUP, UNIT-DOSE 30 ml Historical