Label: REGULAR STRENGTH ANTACID ANTIGAS- aluminum hydroxide, magnesium hydroxide, simethicone liquid

  • NDC Code(s): 63868-134-12
  • Packager: Chain Drug Marketing Association Inc.
  • Category: HUMAN OTC DRUG LABEL

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Drug Label Information

Updated July 29, 2022

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  • ACTIVE INGREDIENTS (in each 10 mL )

    Aluminum hydroxide (equiv. to dried gel, USP) 400 mg
    Magnesium hydroxide 400 mg
    Simethicone 40 mg

  • PURPOSE

    Antacid
    Antacid
    Antigas

  • USE(S)

    relieves:


    • acid indigestion
    • heartburn
    • sour stomach
    • upset stomach and gas associated with these symptoms 
  • WARNINGS

    Do not take more than 80 mL in a 24-hour period, or use the maximum dosage of this product for more than 2 weeks, except under the advice and supervision of a doctor.

  • ASK A DOCTOR BEFORE USE IF YOU HAVE

    • kidney disease
    • a magnesium-restricted diet
  • ASK A DOCTOR OR PHARMACIST BEFORE USE IF YOU ARE 

    • presently taking a prescription drug. Antacids may interact with certain prescription drugs.
  • STOP USE AND ASK DOCTOR

    if symptoms last more than two weeks

  • KEEP OUT OF REACH OF CHILDREN

    .

  • DIRECTIONS

    • shake well before use
    • adults and children 12 years and older: take 10 mL to 20 mL four times a day, or as directed by a doctor
    • children under 12 years: consult a doctor
    • mL = milliliter
  • OTHER INFORMATION

    • each 10 mL contains: magnesium 170 mg, sodium 5 mg
    • store at 20ºC-25ºC (68º-77ºF)
    • do not freeze
  • INACTIVE INGREDIENTS

    ethyl alcohol, flavor, glycerin, hydroxyethyl cellulose, methylparaben, propylene glycol, propylparaben, purified water, saccharin sodium, simethicone emulsion, sorbitol

  • PRINCIPAL DISPLAY PANEL

    NDC 63868-134-12
    Regular strength 

     Antacid Liquid

     Antacid & Antigas

    Aluminum Hydroxide 400mg

    Magnesium Hydroxide 400mg

    Simethicone 40mg

     Relieves:

    • Acid Indigestion
    • Heartburn
    • Sour Stomach
    • Pressure & Bloating


    Mint Flavor
    12 FL OZ (355 mL)


    QC-503-355mL

  • INGREDIENTS AND APPEARANCE
    REGULAR STRENGTH ANTACID ANTIGAS 
    aluminum hydroxide, magnesium hydroxide, simethicone liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:63868-134
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0) (ALUMINUM HYDROXIDE - UNII:5QB0T2IUN0) ALUMINUM HYDROXIDE400 mg  in 10 mL
    MAGNESIUM HYDROXIDE (UNII: NBZ3QY004S) (MAGNESIUM CATION - UNII:T6V3LHY838) MAGNESIUM HYDROXIDE400 mg  in 10 mL
    DIMETHICONE (UNII: 92RU3N3Y1O) (DIMETHICONE - UNII:92RU3N3Y1O) DIMETHICONE40 mg  in 10 mL
    Inactive Ingredients
    Ingredient NameStrength
    ALCOHOL (UNII: 3K9958V90M)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    HYDROXYETHYL CELLULOSE (2000 MPA.S AT 1%) (UNII: S38J6RZN16)  
    METHYLPARABEN (UNII: A2I8C7HI9T)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    PROPYLPARABEN (UNII: Z8IX2SC1OH)  
    WATER (UNII: 059QF0KO0R)  
    SACCHARIN SODIUM (UNII: SB8ZUX40TY)  
    SORBITOL (UNII: 506T60A25R)  
    Product Characteristics
    ColorWHITEScore    
    ShapeSize
    FlavorMINTImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:63868-134-12355 mL in 1 BOTTLE; Type 0: Not a Combination Product07/28/2022
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC MONOGRAPH FINALpart33107/28/2022
    Labeler - Chain Drug Marketing Association Inc. (011920774)