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 9 of 36 · 719 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Rolaids Ultra Strength Antacid Strawberry CALCIUM CARBONATE AND MAGNESIUM HYDROXIDE Chattem, Inc. f4a91efc-2d81-4605-8178-d36ab6c71563 2026-01-14 Warnings Exact identifier application number: M001 D-D SUDIUM BICARBONATE U.S.P. BICARBONATO DE SODA PURO SODIUM BICARBONATE Evi Labs 485f9eb1-6535-c47c-e063-6394a90ae32c 2026-01-14 Warnings Exact identifier application number: M001 Rolaids Extra Strength Fruit CALCIUM CARBONATE AND MAGNESIUM HYDROXIDE Chattem, Inc. ce2af1a6-0387-41e5-ad06-85b790bd4120 2026-01-14 Warnings Exact identifier application number: M001 Rolaids Ultra Strength Mint CALCIUM CARBONATE AND MAGNESIUM HYDROXIDE Chattem, Inc. 8806c912-ab83-4f45-ac78-e826bb3143d4 2026-01-14 Warnings Exact identifier application number: M001 Rolaids Advanced Antacid Anti-gas Wild Berry CALCIUM CARBONATE AND MAGNESIUM HYDROXIDE AND SIMETHICONE Chattem, Inc. 07649a83-0123-4bb5-b130-3067c7d052c5 2026-01-14 Warnings Exact identifier application number: M001 CVS Health Extra Strength Sugar Free Antacid ANTACID CVS Pharmacy,Inc. f722e7ce-6cca-4850-a230-7510c7ca7754 2026-01-12 Warnings Exact identifier application number: M001 MGC Health Calcium Carbonate Antacid Assorted Fruits CALCIUM CARBONATE Medical Group Care LLC 47e1a46c-5665-ac4c-e063-6294a90a9b81 2026-01-08 Warnings Exact identifier application number: M001 MGC Health Calcium Carbonate Antacid Assorted Fruits CALCIUM CARBONATE Medical Group Care LLC 47e19b30-3784-ad98-e063-6294a90aa566 2026-01-08 Warnings Exact identifier application number: M001 MGC Health Calcium Carbonate Antacid Tropical Fruit CALCIUM CARBONATE Medical Group Care LLC 47e1bc32-baf5-ad9a-e063-6294a90ad5b4 2026-01-08 Warnings Exact identifier application number: M001 MGC Health Calcium Carbonate Antacid Assorted Berries CALCIUM CARBONATE Medical Group Care LLC 47e1c7c7-4f3b-c04b-e063-6394a90a775f 2026-01-08 Warnings Exact identifier application number: M001 Sanar Baking Soda 8oz 100% pure SODIUM BICARBONATE Evi Labs 47e7f801-3176-288c-e063-6394a90abef4 2026-01-08 Warnings Exact identifier application number: M001 Xpect Antacid CALCIUM CARBONATE Cintas Corporation 3ef4eac7-cc9d-4ee2-b93a-59b85dbc6e7c 2026-01-08 Warnings Exact identifier application number: M001 DR. SANA BICARBONATO DE SODIO 4 Fl oz and 6 Floz SODIUM BICARBONATE Evi Labs 47330d09-7db1-254d-e063-6294a90ae7de 2026-01-07 Warnings Exact identifier application number: M001 DE LA CRUZ SODIUM BICARBONATE ANTACID SODIUM BICARBONATE DLC Laboratories, Inc. fc469943-9749-45ee-93f7-90fdbcdc7215 2026-01-07 Warnings Exact identifier application number: M001 De La Cruz Desempacho SODIUM BICARBONATE DLC LABORATORIES, INC. 741e105a-3ed2-4fc7-ab06-273e515a2d16 2026-01-07 Warnings Exact identifier application number: M001 ANTACID AND ANTIGAS CALCIUM CARBONATE, MAGNESIUM HYDROXIDE, SIMETHICONE Geri-Care Pharmaceuticals, Corp 472eafe8-aa7a-f435-e063-6294a90acf6b 2025-12-30 Warnings Exact identifier application number: M001 ANTACID AND ANTIGAS CALCIUM CARBONATE, MAGNESIUM HYDROXIDE, SIMETHICONE Geri-Care Pharmaceuticals, Corp 472f5bfc-c676-56da-e063-6294a90a74af 2025-12-30 Warnings Exact identifier application number: M001 ANTACID AND ANTIGAS CALCIUM CARBONATE, MAGNESIUM HYDROXIDE, SIMETHICONE Geri-Care Pharmaceuticals, Corp 472ffa66-938f-14e7-e063-6394a90ad0ca 2025-12-30 Warnings Exact identifier application number: M001 QC Ultra Strength Antacid Soft Chews, Cherry QC ANTACID SOFT CHEWS, CHERRY Xiamen Kang Zhongyuan Biotechnology Co., Ltd. 26a97517-d3e7-d896-e063-6394a90acc95 2025-12-29 Warnings Exact identifier application number: M001 Tums Chewy Bites CALCIUM CARBONATE Select Consumer Group 3caa037e-3424-f9ce-e063-6294a90ac1e8 2025-12-27 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