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 26 of 34 · 678 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Regular Strength Antacid Mint ALUMINUM HYDROXIDE, MAGNESIUM HYDROXIDE, SIMETHICONE Topco Associates, LLC 59c16c09-c23d-4a37-8460-d6c00a268ed5 2024-12-26 Warnings Exact identifier application number: M001 ANTACID CALCIUM CARBONATE Advance Pharmaceutical Inc. face4e8c-3d0f-4c2e-83c1-44397b225ae7 2024-12-26 Warnings Exact identifier application number: M001 ANTACID CALCIUM CARBONATE Advance Pharmaceutical Inc. 3203dfc5-2cb1-4703-8d81-63fba07ddd98 2024-12-26 Warnings Exact identifier application number: M001 Magnesium Oxide MAGNESIUM OXIDE Richmond Pharmaceuticals, Inc. 9119b7f0-3e8a-7be7-e053-2995a90a4634 2024-12-26 Warnings Exact identifier application number: M001 Magnesium Oxide MAGNESIUM OXIDE Richmond Pharmaceuticals, Inc. db5941b2-0a04-452a-8fbc-bd5e40fadfb1 2024-12-26 Warnings Exact identifier application number: M001 HEB Extra Strength Smooth Antacid Assorted Fruits CALCIUM CARBONATE H E B 2faac316-7b59-4df8-b751-37069e865263 2024-12-26 Warnings Exact identifier application number: M001 Good Neighbor Pharmacy Antacid Extra Strength CALCIUM CARBONATE AmerisourceBergen Drug Corporation 5e3a3c20-dabe-4427-9e75-99759905caa0 2024-12-26 Warnings Exact identifier application number: M001 Maximum Strength Antacid Cherry liquid ALUMINUM HYDROXIDE, MAGNESIUM HYDROXIDE, SIMETHICONE Topco Associates, LLC 31d2e77d-5eda-4f47-917c-3390d6c782af 2024-12-26 Warnings Exact identifier application number: M001 Maximum Strength Antacid Mint ALUMINUM HYDROXIDE, MAGNESIUM HYDROXIDE, SIMETHICONE Topco Associates, LLC 50ceff1e-b6df-40f8-89f3-667cc8f9e750 2024-12-26 Warnings Exact identifier application number: M001 HEB Extra Strength Smooth Antacid Peppermint CALCIUM CARBONATE H E B d04e691e-6d1c-4c39-9504-7ac0f1bd197d 2024-12-26 Warnings Exact identifier application number: M001 Antacid ALUMINUM HYDROXIDE, MAGNESIUM HYDROXIDE, SIMETHICONE H E B f294cf44-fb21-4b2e-8b7c-efd41416c6b2 2024-12-26 Warnings Exact identifier application number: M001 Antacid CALCIUM CARBONATE Trifecta Pharmaceuticals USA LLC 14a7916e-5363-7f1b-e063-6294a90a20aa 2024-12-20 Warnings Exact identifier application number: M001 maximum strength antacid cherry ALUMINUM HYDROXIDE, MAGNESIUM HYDROXIDE, SIMETHICONE UNITED NATURAL FOODS, INC. DBA UNFI d6b49f0a-cf05-4b1b-8cad-c5795aa31645 2024-12-20 Warnings Exact identifier application number: M001 GOODSENSE Ultra Strength Antacid Peppermint CALCIUM CARBONATE GoodSense 04950b56-7760-4b6c-8110-86b6a3f795b4 2024-12-19 Warnings Exact identifier application number: M001 Goodsense Regular Strength Antacid Peppermint CALCIUM CARBONATE GoodSense 32c04f3e-59f3-44aa-ad92-672444982710 2024-12-19 Warnings Exact identifier application number: M001 GOODSENSE Ultra Strength Antacid Assorted Fruit CALCIUM CARBONATE GoodSense ad4d51f6-b55b-45db-b034-fb3da54fbe99 2024-12-19 Warnings Exact identifier application number: M001 TUMS Extra Strength Sugar-Free CALCIUM CARBONATE Haleon US Holdings LLC 3495102f-55d2-4a94-8d55-f46f49e00c27 2024-12-19 Warnings Exact identifier application number: M001 Goodsense Extra Strength Antacid Assorted Fruit CALCIUM CARBONATE GoodSense ae6270fc-0f8d-4bba-8f12-adba3f07f7c5 2024-12-19 Warnings Exact identifier application number: M001 Quality Choice Extra Strength Assorted Berry Antacid Extra strength Assorted Berry Antacid CALCIUM CARBONATE Chain Drug Marketing Association Inc. ec729051-72d3-4d1a-8e39-d4495d5c1cf3 2024-12-18 Warnings Exact identifier application number: M001 Guardian Extra Strength Antacid CALCIUM CARBONATE Guardian Drug Company aef3d830-c5c3-4f72-86ba-d31945a756db 2024-12-18 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