Magnesium Oxide

Manufacturer
Bryant Ranch Prepack
Effective date
2022-04-20
Label type
HUMAN OTC DRUG LABEL
Version
101
Source
legacy-cache
Hydrated at
2026-08-01 22:02:48

Label at a glance#

ProductMagnesium Oxide
Active ingredientMAGNESIUM OXIDE
Label structure10 sections

Dosage and administration

Take one tablet daily or as directed by a physician.

Storage and handling

Keep tightly closed and store in a cool, dry place.

Label contents#

Full prescribing information#

Active ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Magnesium Oxide 

Purpose

OTC - PURPOSE SECTION

Magnesium Oxide may help in magnesium deficiencies †

Use(s)

INDICATIONS & USAGE SECTION

As a dietary supplement.

Warnings

WARNINGS SECTION

Do not use

OTC - DO NOT USE SECTION

Do not take this product if you are presently taking a prescription drug without consulting your physician or other health care professional. If you have kidney disease, take only under the supervision of a physician. May have a laxative effect.

Pregnancy/Breastfeeding

OTC - PREGNANCY OR BREAST FEEDING SECTION

ask a health professional before use.

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Directions

DOSAGE & ADMINISTRATION SECTION

Take one tablet daily or as directed by a physician.

Other information

SPL UNCLASSIFIED SECTION

This product is sealed for your protection. Do not use if imprinted safety seal under cap is broken or missing.

Storage

STORAGE AND HANDLING SECTION

Keep tightly closed and store in a cool, dry place.

Inactive ingredients

INACTIVE INGREDIENT SECTION

colloidal silicon dioxide, croscarmellose sodium, microcrystalline cellulose, stearic acid.

HOW SUPPLIED

How Supplied Section

NDC: 63629-2217-1: 100 Tablets in a BOTTLE

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Magnesium Oxide 420 mgTablet, #100

Label
Label

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
63629-2217-12024-09-23C16284748780-11030e365-487e-111a-e063-dadaa90a10e2306-Magnesium Oxide 420mg
63629-2217-12024-01-30C16284748780-11030e365-487e-111a-e063-dadaa90a10e2306-Magnesium Oxide 420mg

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
63629-2217-1EA - Each63629-2217be140003-464a-4ae8-9f57-e2ec9a862e6012021-07-15
0603-0213-21EA - Each0603-02134715cc13-8d2e-4aaf-a431-5366461f821312013-02-13

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
63629-221763629-2217-1
0603-0213

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Source Document#

Source XML

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 · 2 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
76641385-9eb8-46e4-8ba6-3aee8a77676207274420-b7fe-4b68-aca5-867db8f22c072024-09-23WarningsExact identifier
spl set id: 07274420-b7fe-4b68-aca5-867db8f22c07
Magnesium OxideMAGNESIUM OXIDEEndo USAd5c123f8-1396-4d8c-96d3-e5ade96a6ef82020-11-10WarningsExact identifier
ndc (product): 0603-0213

Reported adverse events (FAERS/openFDA)#

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