MAGNESIUM OXIDE- magnesium oxide tablet 
Wittman Pharma, Inc.

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Mag Oxide

Tablet taken Orally

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

Ask a doctor before use if:

* you have kidney disease

* you are taking a prescription drug (antacids may interact with certain prescription drugs)

* you are pregnant or breast feeding

Microcrystaline Cellulose,

Sodium Starch Glycolate,

Stearic Acid

relieves acid indigestion and upset stomach

Keep out of reach of children

Antacid

Active Ingredient (in each tablet)

Magnesium Oxide 400 mg (241.3 mg Elemental Magnesium)

Drug Facts

ACTIVE INGREDIENT (In each tablet)

Magnesium Oxide 400mg (241.3mg elemental magnesium)

Purpose

Antacid

USES

relieves - acid indigestion - upset stomach

WARNINGS

Ask a doctor before use if:

You have kidney disease

You are taking a prescription drug (antacids may interact with certain prescription drugs).

You are pregnant or breast feeding.

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

May have a laxative effect.

Keep out of reach of children.

DIRECTIONS

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

OTHER INFORMATION

Magnesium content per tablet: 241.3mg

store at room temperature 59°- 86° F (15°- 30°C)

INACTIVE INGREDIENTS

microcrystalline cellulose, sodium starch, glyocolate, stearic acid

Questions?

1-352-549-9917 M-F 9am - 5pm EST

Mag Label

MAGNESIUM OXIDE 
magnesium oxide tablet
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:83335-001
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
MAGNESIUM OXIDE (UNII: 3A3U0GI71G) (MAGNESIUM CATION - UNII:T6V3LHY838) MAGNESIUM CATION241.3 mg  in 1000 mg
Inactive Ingredients
Ingredient NameStrength
SODIUM STARCH GLYCOLATE TYPE A POTATO (UNII: 5856J3G2A2)  
STEARIC ACID (UNII: 4ELV7Z65AP)  
CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)  
Product Characteristics
Colorwhite (White to Off-White) Scorescore with uneven pieces
ShapeROUND (Tablet) Size4mm
FlavorImprint Code MG
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:83335-001-12120 mg in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product03/16/2023
Image of Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM00103/16/2023
Labeler - Wittman Pharma, Inc. (830980947)
Registrant - Wittman Pharma, Inc. (830980947)
Establishment
NameAddressID/FEIBusiness Operations
Wittman Pharma, Inc.830980947manufacture(83335-001) , analysis(83335-001) , label(83335-001)

Revised: 4/2024
Document Id: 1547fd77-3c10-152a-e063-6394a90a8688
Set id: f7064d17-04b1-160b-e053-6394a90ad8be
Version: 5
Effective Time: 20240404
 
Wittman Pharma, Inc.