Label: MAGNESIUM OXIDE tablet

  • NDC Code(s): 69367-298-20
  • Packager: Westminster Pharmaceuticals, LLC
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated October 19, 2020

If you are a consumer or patient please visit this version.

  • SPL UNCLASSIFIED SECTION

    Drug Facts

  • Active Ingredient

    Magnesium Oxide 400 mg (241.3 mg Elemental Magnesium)

  • Purpose

    Antacid

  • Use

    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

    • 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

    Corn Starch, Croscarmellose Sodium, Magnesium Stearate, Microcrystalline Cellulose, Silicon Dioxide, Stearic Acid.

  • Questions?

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

  • PRINCIPAL DISPLAY PANEL - 400 mg Tablet Bottle Label

    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
  • INGREDIENTS AND APPEARANCE
    MAGNESIUM OXIDE 
    magnesium oxide tablet
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69367-298
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    MAGNESIUM OXIDE (UNII: 3A3U0GI71G) (MAGNESIUM CATION - UNII:T6V3LHY838) MAGNESIUM CATION400 mg
    Inactive Ingredients
    Ingredient NameStrength
    MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)  
    CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)  
    STARCH, CORN (UNII: O8232NY3SJ)  
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
    STEARIC ACID (UNII: 4ELV7Z65AP)  
    MAGNESIUM STEARATE (UNII: 70097M6I30)  
    Product Characteristics
    ColorWHITEScore2 pieces
    ShapeROUNDSize11mm
    FlavorImprint Code AM3
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:69367-298-20120 in 1 BOTTLE; Type 0: Not a Combination Product10/15/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC MONOGRAPH DRUGM00110/15/2020
    Labeler - Westminster Pharmaceuticals, LLC (079516651)