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Magnesium Oxide

NDC 69367-298, Magnesium Oxide, tablet, from Westminster Pharmaceuticals, LLC.

Product NDC
69367-298
Status
Listed
Labeler
Westminster Pharmaceuticals, LLC
Dosage form
TABLET
Route
ORAL
Product type
HUMAN OTC DRUG
Marketing category
OTC MONOGRAPH DRUG
Application
M001
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/69367-298 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • MAGNESIUM OXIDE400 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]

Package NDCNDC-11Package
69367-298-2069367029820120 TABLET in 1 BOTTLE (69367-298-20)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • NADAC price for package 69367029820

    GET /v1/drugs/nadac/69367029820

Use it

Look up 69367-298 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/69367-298 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 69367-298. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
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Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.