Magnesium Oxide

openFDA label record#

This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.

Verified complete openFDA source JSON (canonical bytes are SHA-256 checked before publication)

Brand name
Magnesium Oxide
Generic name
MAGNESIUM OXIDE
Manufacturer
Richmond Pharmaceuticals, Inc.
Product type
HUMAN OTC DRUG
SPL set ID
9119b7f0-3e8a-7be7-e053-2995a90a4634
SPL ID
2a329845-3f50-540c-e063-6394a90af0a9
Version
13
Effective date
2024-12-26
Source export date
2026-10-30
Source partition
11
Source file
https://download.open.fda.gov/drug/label/drug-label-0011-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-30/9abf0f8b126f8aad070e21ea702bfb5e39ce670b16ae57dd52e8877705d1bf5d/drug-label-0011-of-0014.json.zip
Source manifest SHA-256
b11f1f6b476c7417db937215bf14307ef1a0b69465b42b411ad52f42ae36ead3
Import run
20261102T182004Z
Imported at
2026-11-02 19:27:03
Harmonized routes table
Harmonized routes
ORAL

Warnings cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Warnings sections page 1 of 1 · 1 matching rows.

warnings

WARNINGS Ask a doctor 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 advise 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.

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.