Home NDC 81033-007 Kesin MAG-AL Plus XS
Product NDC 81033-007
11-digit product format 810330007
Labeler code 81033
Product ID 81033-007_515185f7-687b-8010-e063-6394a90a1439
Type HUMAN OTC DRUG
Nonproprietary name Aluminum and Magnesium Hydroxide w/Simethicone Suspension
Dosage form SUSPENSION
Route ORAL
Labeler Kesin Pharma Corporation
Application M001
Marketing category OTC MONOGRAPH DRUG
Marketing start 2025-11-05
Substance DIMETHICONE, UNSPECIFIED; ALUMINUM HYDROXIDE; MAGNESIUM HYDROXIDE
Active strength 40; 400; 400 mg/5mL; 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], Skin Barrier Activity [PE], 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 Plus XS
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength DIMETHICONE, UNSPECIFIED 40 mg/5mL ALUMINUM HYDROXIDE 400 mg/5mL MAGNESIUM HYDROXIDE 400 mg/5mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 3 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 92RU3N3Y1O Internal UNII lookup 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 237870 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 81033-007-01 Kesin MAG-AL Plus XS 100 in 1 CASE SUSPENSION 100 2 81033-007-30 Kesin MAG-AL Plus XS 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 10 of 34 · 678 matching rows.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 81033-007-01 81033000701 100 CUP, UNIT-DOSE in 1 CASE (81033-007-01) / 30 mL in 1 CUP, UNIT-DOSE (81033-007-30) 2025-11-05 No No Current 81033-007-30 81033000730 30 mL in 1 CUP, UNIT-DOSE 30 ml Historical