Label: GAVISCON- aluminum hydroxide and magnesium carbonate liquid

  • NDC Code(s): 0135-0094-41, 0135-0094-42, 0135-0095-41, 0135-0574-01
  • Packager: Haleon US Holdings LLC
  • Category: HUMAN OTC DRUG LABEL

Drug Label Information

Updated September 26, 2025

If you are a healthcare professional or from the pharmaceutical industry please visit this version.

  • Active ingredients (in each 15 mL tablespoonful) Regular Strength

    Aluminum hydroxide 95 mg

    Magnesium carbonate 358 mg

  • Active ingredients (in each 5 mL / teaspoonful) Extra Strength

    Aluminum hydroxide 254 mg

    Magnesium carbonate 237.5 mg

  • Purposes

    Antacid

    Antacid

  • Uses

    relieves

    heartburn
    acid indigestion
    sour stomach
    upset stomach associated with these symptoms
  • Warnings

    Ask a doctor or pharmacist before use if you

    have kidney disease
    are on a sodium-restricted diet or a magnesium-restricted diet
    are taking a prescription drug. Antacids may interact with certain prescription drugs.

    When using this product (Regular Strength)

    do not take more than 8 tablespoonfuls in 24 hours
    do not use the maximum dosage for more than 2 weeks except under the advice and supervision of a doctor
    laxative effect may occur

    When using this product (Extra Strength)

    do not take more than 16 teaspoonfuls in 24 hours
    do not use the maximum dosage for more than 2 weeks, except under the advice and supervision of a doctor
    laxative effect may occur

    Keep out of reach of children.

    In case of overdose, get medical help or contact a Poison Control Center right away.

  • Directions (Regular Strength)

    shake well
    take 1-2 tablespoonfuls four times a day or as directed by a doctor
    take after meals and at bedtime
    dispense product only by spoon or other measuring device
  • Directions (Extra Strength)

    shake well
    take 2-4 teaspoonfuls four times a day or as directed by a doctor
    take after meals and at bedtime
    dispense product only by spoon or other measuring device
  • Other information (Regular Strength)

    each tablespoon (15 mL) contains: magnesium 115 mg, sodium 52 mg
    store at up to 25°C (77°F). Avoid freezing.
    keep tightly closed
  • Other information (Extra Strength)

    each teaspoon (5 mL) contains: magnesium 75 mg, sodium 11 mg
    store at up to 25°C (77°F). Avoid freezing.
    keep tightly closed
  • Inactive ingredients (Regular Strength)

    benzyl alcohol, D&C yellow #10, edetate disodium, FD&C blue #1, flavor, glycerin, saccharin sodium, sodium alginate, sorbitol solution, water, xanthan gum

  • Inactive ingredients (Extra Strength Cool Mint)

    benzyl alcohol, edetate disodium, glycerin, natural and artificial flavors, purified water, simethicone emulsion, sodium alginate, sodium saccharin, sorbitol solution, xanthan gum

  • Inactive ingredients (Extra Strength Cherry)

    benzyl alcohol, edetate disodium, glycerin, natural and artificial flavors, purified water, simethicone emulsion, sodium alginate, sodium saccharin, sorbitol solution, xanthan gum

  • Questions or comments?

    1-800-452-0051

  • Additional Information

    Do not use if printed inner safety seal under cap is broken or missing.

    Trademarks are owned by or licensed to the Haleon group of companies.

    ©2025 Haleon group of companies or its licensor.

    Pat. Info www.productpats.com

    Distributed by:

    Haleon

    Warren, NJ 07059

    Made in Mexico

  • Principal Display Panel

    NDC 0135-0094-41

    Gaviscon

    LIQUID ANTACID

    REGULAR STRENGTH

    Fast-Acting Heartburn Relief
    Helps Keep Acid Down for Hours

    COOL MINT

    FLAVOR

    12 FL OZ (355 mL)

    FRONT: 00067473

    BACK: 00067474

    00067473 Gaviscon Regular Strength 12 fl oz
  • Principal Display Panel

    HALEON

    Gaviscon

    LIQUID ANTACID

    EXTRA STRENGTH

    Fast-Acting Heartburn Relief
    Helps Keep Acid Down for Hours

    COOL MINT
    FLAVOR

    12 FL OZ (355 mL)

    FRONT: 00213316

    BACK: 00213317

    Gaviscon Extra Strength Cool Mint 12 fl oz label.jpg
  • Principal Display Panel

    HALEON

    Gaviscon

    LIQUID ANTACID

    EXTRA STRENGTH

    Fast-Acting Heartburn Relief
    Helps Keep Acid Down for Hours

    CHERRY
    FLAVOR

    12 FL OZ (355 mL)

    FRONT: 00213320

    BACK: 00213322

    Gaviscon Extra Strength 12 fl oz label.jpg
  • INGREDIENTS AND APPEARANCE
    GAVISCON 
    aluminum hydroxide and magnesium carbonate liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0135-0094
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0) (ALUMINUM HYDROXIDE - UNII:5QB0T2IUN0) ALUMINUM HYDROXIDE95 mg  in 15 mL
    MAGNESIUM CARBONATE (UNII: 0E53J927NA) (CARBONATE ION - UNII:7UJQ5OPE7D) MAGNESIUM CARBONATE358 mg  in 15 mL
    Inactive Ingredients
    Ingredient NameStrength
    BENZYL ALCOHOL (UNII: LKG8494WBH)  
    EDETATE DISODIUM (UNII: 7FLD91C86K)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    WATER (UNII: 059QF0KO0R)  
    SODIUM ALGINATE (UNII: C269C4G2ZQ)  
    SACCHARIN SODIUM (UNII: SB8ZUX40TY)  
    SORBITOL (UNII: 506T60A25R)  
    XANTHAN GUM (UNII: TTV12P4NEE)  
    Product Characteristics
    ColorGREENScore    
    ShapeSize
    FlavorMINT (cool mint) Imprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0135-0094-41355 mL in 1 BOTTLE; Type 0: Not a Combination Product01/14/2011
    2NDC:0135-0094-42177 mL in 1 BOTTLE; Type 0: Not a Combination Product01/14/2011
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00101/14/2011
    GAVISCON 
    aluminum hydroxide and magnesium carbonate liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0135-0095
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0) (ALUMINUM HYDROXIDE - UNII:5QB0T2IUN0) ALUMINUM HYDROXIDE254 mg  in 5 mL
    MAGNESIUM CARBONATE (UNII: 0E53J927NA) (CARBONATE ION - UNII:7UJQ5OPE7D) MAGNESIUM CARBONATE237.5 mg  in 5 mL
    Inactive Ingredients
    Ingredient NameStrength
    BENZYL ALCOHOL (UNII: LKG8494WBH)  
    DIMETHICONE, UNSPECIFIED (UNII: 92RU3N3Y1O)  
    EDETATE DISODIUM (UNII: 7FLD91C86K)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    SACCHARIN SODIUM (UNII: SB8ZUX40TY)  
    SODIUM ALGINATE (UNII: C269C4G2ZQ)  
    SORBITOL (UNII: 506T60A25R)  
    XANTHAN GUM (UNII: TTV12P4NEE)  
    WATER (UNII: 059QF0KO0R)  
    Product Characteristics
    ColorWHITEScore    
    ShapeSize
    FlavorMINT (cool mint) Imprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0135-0095-41355 mL in 1 BOTTLE; Type 0: Not a Combination Product01/14/2011
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00101/14/2011
    GAVISCON 
    aluminum hydroxide and magnesium carbonate liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0135-0574
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0) (ALUMINUM HYDROXIDE - UNII:5QB0T2IUN0) ALUMINUM HYDROXIDE254 mg  in 5 mL
    MAGNESIUM CARBONATE (UNII: 0E53J927NA) (CARBONATE ION - UNII:7UJQ5OPE7D) MAGNESIUM CARBONATE237.5 mg  in 5 mL
    Inactive Ingredients
    Ingredient NameStrength
    BENZYL ALCOHOL (UNII: LKG8494WBH)  
    DIMETHICONE, UNSPECIFIED (UNII: 92RU3N3Y1O)  
    EDETATE DISODIUM (UNII: 7FLD91C86K)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    SACCHARIN SODIUM (UNII: SB8ZUX40TY)  
    SODIUM ALGINATE (UNII: C269C4G2ZQ)  
    SORBITOL (UNII: 506T60A25R)  
    WATER (UNII: 059QF0KO0R)  
    XANTHAN GUM (UNII: TTV12P4NEE)  
    Product Characteristics
    ColorWHITEScore    
    ShapeSize
    FlavorCHERRYImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0135-0574-01355 mL in 1 BOTTLE; Type 0: Not a Combination Product08/01/2014
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00108/01/2014
    Labeler - Haleon US Holdings LLC (079944263)