Magnesium Oxide

Manufacturer
Westminster Pharmaceuticals, LLC
Effective date
2026-07-06
Label type
HUMAN OTC DRUG LABEL
Version
16
Source
daily-update
Hydrated at
2026-07-25 05:10:26

Label at a glance#

ProductMagnesium Oxide
Active ingredientMAGNESIUM OXIDE
Label structure10 sections

Dosage and administration

take one or two antacid tablets daily. Do not exceed two tablets unless directed by a physician.

Storage and handling

Store at controlled room temperature 15° to 30°C (59° to 86°F). Tamper evident, do not use if imprinted safety seal under cap is broken or missing.

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Magnesium Oxide 400 mg (241.3 mg Elemental Magnesium)

Purpose

OTC - PURPOSE SECTION

Antacid

Use

INDICATIONS & USAGE SECTION

relieves:

  • acid indigestion
  • upset stomach

Warnings

WARNINGS SECTION

Ask a doctor before use if

OTC - ASK DOCTOR SECTION

  • you have kidney disease
  • you are taking a prescription drug (antacids may interact with certain prescription drugs)
  • you are pregnant or breast feeding.

OTC - DO NOT USE SECTION

Do not take more than 2 tablets in a 24 hour period.

  • May have a laxative effect.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

Directions

DOSAGE & ADMINISTRATION SECTION

  • take one or two antacid tablets daily. Do not exceed two tablets unless directed by a physician.

Other Information

STORAGE AND HANDLING SECTION

  • Store at controlled room temperature 15° to 30°C (59° to 86°F).
  • Tamper evident, do not use if imprinted safety seal under cap is broken or missing.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Colloidal Silicon Dioxide, Corn Starch, Croscarmellose Sodium, Microcrystalline Cellulose, and Stearic Acid.

Questions?

OTC - QUESTIONS SECTION

Call 1-844-221-7294 M-F 9am - 5pm EST

PRINCIPAL DISPLAY PANEL - 400 mg Tablet Bottle Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC 69367-298-20

Magnesium
Oxide 400 mg

241.3 mg Elemental Magnesium
Antacid

Sugar and Gluten Free

120 Tablets

Westminster
Pharmaceuticals

PRINCIPAL DISPLAY PANEL - 400 mg Tablet Bottle Label
PRINCIPAL DISPLAY PANEL - 400 mg Tablet Bottle Label

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
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Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
69367-29869367-298-20

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
152026-07-06weekly-update2026-07-17 21:44:02
132025-08-05full-release2026-06-01 01:09:47

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Magnesium OxideMAGNESIUM OXIDEWestminster Pharmaceuticals, LLC52eeac0e-94bb-48c3-81dc-578e96406c012026-07-06WarningsExact identifier
ndc (package): 69367-298-20
ndc (product): 69367-298
ndc11 (package): 69367029820
spl id: 7afa67e6-50ba-4aac-9607-d38b690e5dc0
spl set id: 52eeac0e-94bb-48c3-81dc-578e96406c01

Reported adverse events (FAERS/openFDA)#

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