magnesium oxide

Generic: magnesium oxide

Labeler: kesin pharma
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name magnesium oxide
Generic Name magnesium oxide
Labeler kesin pharma
Dosage Form TABLET
Routes
ORAL
Active Ingredients

magnesium oxide 400 mg/1

Manufacturer
Kesin Pharma

Identifiers & Regulatory

Product NDC 81033-027
Product ID 81033-027_4225e628-15ad-6bf0-e063-6394a90a98d6
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M001
Listing Expiration 2026-12-31
Marketing Start 2025-04-07

Pharmacologic Class

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]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 81033027
Hyphenated Format 81033-027

Supplemental Identifiers

RxCUI
198741
UPC
0381033027128
UNII
3A3U0GI71G

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name magnesium oxide (source: ndc)
Generic Name magnesium oxide (source: ndc)
Application Number M001 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 400 mg/1
source: ndc
Packaging
  • 10 BLISTER PACK in 1 CARTON (81033-027-01) / 100 TABLET in 1 BLISTER PACK (81033-027-41)
  • 120 TABLET in 1 BOTTLE (81033-027-12)
source: ndc

Packages (2)

81033-027-01 10 BLISTER PACK in 1 CARTON (81033-027-01) / 100 TABLET in 1 BLISTER PACK (81033-027-41) 81033-027-12 120 TABLET in 1 BOTTLE (81033-027-12)

Ingredients (1)

magnesium oxide (400 mg/1)

Linked Drug Pages (1)

Magnesium Oxide ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "4225e628-15ad-6bf0-e063-6394a90a98d6", "openfda": {"upc": ["0381033027128"], "unii": ["3A3U0GI71G"], "rxcui": ["198741"], "spl_set_id": ["31f417f0-1637-eefa-e063-6294a90a121b"], "manufacturer_name": ["Kesin Pharma"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 BLISTER PACK in 1 CARTON (81033-027-01)  / 100 TABLET in 1 BLISTER PACK (81033-027-41)", "package_ndc": "81033-027-01", "marketing_start_date": "20251101"}, {"sample": false, "description": "120 TABLET in 1 BOTTLE (81033-027-12)", "package_ndc": "81033-027-12", "marketing_start_date": "20250407"}], "brand_name": "Magnesium Oxide", "product_id": "81033-027_4225e628-15ad-6bf0-e063-6394a90a98d6", "dosage_form": "TABLET", "pharm_class": ["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]"], "product_ndc": "81033-027", "generic_name": "Magnesium Oxide", "labeler_name": "Kesin Pharma", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Magnesium Oxide", "active_ingredients": [{"name": "MAGNESIUM OXIDE", "strength": "400 mg/1"}], "application_number": "M001", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20250407", "listing_expiration_date": "20261231"}