Home NDC 81033-027 Magnesium Oxide
Product NDC 81033-027
11-digit product format 810330027
Labeler code 81033
Product ID 81033-027_4225e628-15ad-6bf0-e063-6394a90a98d6
Type HUMAN OTC DRUG
Nonproprietary name Magnesium Oxide
Dosage form TABLET
Route ORAL
Labeler Kesin Pharma
Application M001
Marketing category OTC MONOGRAPH DRUG
Marketing start 2025-04-07
Substance MAGNESIUM OXIDE
Active strength 400 mg/1
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 2026-12-31
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.
Warnings cross-check# openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
warnings Warnings Ask a doctor before use if you have kidney disease Ask a doctor or pharmacist before use if you are taking a prescription drug. Antacids may interact with certain prescription drugs. Do not take more than 2 tablets in a 24 hour period or use the maximum dosage of this product for more than two weeks, except under the advice and supervision of a physician. May have a laxative effect. If pregnant or breast-feeding, ask a health professional before use. Keep out of reach of children.
Additional Listing Data#
Finished product Yes
Brand name base Magnesium Oxide
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength MAGNESIUM OXIDE 400 mg/1
Harmonized Identifiers# Field, Values table Field Values Unii 3A3U0GI71G Rxcui 198741
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 81033-027-01 Magnesium Oxide 10 in 1 CARTON TABLET 10 2 81033-027-12 Magnesium Oxide 120 in 1 BOTTLE TABLET 120 2 81033-027-41 Magnesium Oxide 100 in 1 BLISTER PACK TABLET 100 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 81033-027-01 81033002701 10 BLISTER PACK in 1 CARTON (81033-027-01) / 100 TABLET in 1 BLISTER PACK (81033-027-41) 10 blister pack 2025-11-01 No No Current 81033-027-12 81033002712 120 TABLET in 1 BOTTLE (81033-027-12) 120 tablet 2025-04-07 No No Current 81033-027-41 81033002741 100 in 1 BLISTER PACK Historical