magnesium oxide
Generic: magnesium oxide
Labeler: method pharmaceuticals, llcDrug Facts
Product Profile
Brand Name
magnesium oxide
Generic Name
magnesium oxide
Labeler
method pharmaceuticals, llc
Dosage Form
TABLET
Routes
Active Ingredients
magnesium oxide 400 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
58657-120
Product ID
58657-120_41b54dc8-16af-7ea0-e063-6394a90ad7b2
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M001
Listing Expiration
2026-12-31
Marketing Start
2018-07-25
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
58657120
Hyphenated Format
58657-120
Supplemental Identifiers
RxCUI
UNII
Packaging Origin
Original Packager
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
source: ndc
Resolved Composition
Strengths
- 400 mg/1
Packaging
- 120 TABLET in 1 BOTTLE (58657-120-12)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "41b54dc8-16af-7ea0-e063-6394a90ad7b2", "openfda": {"unii": ["3A3U0GI71G"], "rxcui": ["198741"], "spl_set_id": ["0af63651-f9d9-43b9-b6f0-4878466a82e6"], "manufacturer_name": ["Method Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "120 TABLET in 1 BOTTLE (58657-120-12)", "package_ndc": "58657-120-12", "marketing_start_date": "20180725"}], "brand_name": "Magnesium Oxide", "product_id": "58657-120_41b54dc8-16af-7ea0-e063-6394a90ad7b2", "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": "58657-120", "generic_name": "Magnesium Oxide", "labeler_name": "Method Pharmaceuticals, LLC", "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": "20180725", "listing_expiration_date": "20261231"}