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 openFDA label cross-check# Cross-check layer: openFDA label JSON enriches search and identifies hydration gaps. The DailyMed Structured Product Label remains the canonical label presentation on FDA.report.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Kesin MAG-AL ALUMINUM AND MAGNESIUM HYDROXIDE SUSPENSION Kesin Pharma Corporation 42df2198-14dc-da1c-e063-6394a90a1ae6 2026-05-08 Warnings Exact identifier
Warnings cross-check# openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
warnings Warnings 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 kidney disease a magnesium-restricted diet Ask a doctor or pharmacist before use if you are presently taking a prescription drug. Antacids may interact with certain prescription drugs. Stop use and ask a doctor if symptoms last more than 2 weeks If pregnant or breast-feeding, ask a health professional before use. Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.
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 Identifiers# Field, Values table Field Values Unii 5QB0T2IUN0, NBZ3QY004S Rxcui 243463
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
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