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 April 4, 2024

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  • 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

  • Purpose

    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 80 mg, sodium 14 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, flavor, glycerin, saccharin sodium, simethicone emulsion, sodium alginate, sorbitol solution, water, xanthan gum

  • Inactive Ingredients (Extra Strength Cherry)

    Benzyl alcohol, edetate disodium, flavor, glycerin, saccharin sodium, simethicone emulsion, sodium alginate, sorbitol solution, water, xanthan gum

  • Questions or comments?

    1-888-367-6471

  • Additional Information

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

    Distributed by:

    GSK Consumer Healthcare

    Warren, NJ 07059

    Made in Mexico

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

    ©2021 GSK group of companies or its licensor.

  • 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

    NDC 0135-0095-41

    Gaviscon

    LIQUID ANTACID

    EXTRA STRENGTH

    • Fast-Acting Heartburn Relief
    • Helps Keep Acid Down for Hours

    COOL MINT

    FLAVOR

    12 FL OZ (355 mL)

    FRONT: 00067475

    BACK: 00067476

    00067475 Gaviscon Extra Strength 12 fl oz
  • Principal Display Panel

    NDC 0135-0574-01

    Gaviscon ®

    EXTRA STRENGTH

    LIQUID ANTACID

    • Fast-Acting Heartburn Relief
    • Helps Keep Acid Down for Hours

    CHERRY

    FLAVOR

    12fl oz (355 ml)

    ©2014 GlaxoSmithKline

    FRONT: 103698XA

    BACK: 103699XA

    Gavison Extra Strength Cherry 12 fl oz (355mL) label
  • 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)  
    D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)  
    EDETATE DISODIUM (UNII: 7FLD91C86K)  
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    SACCHARIN SODIUM (UNII: SB8ZUX40TY)  
    SODIUM ALGINATE (UNII: C269C4G2ZQ)  
    SORBITOL (UNII: 506T60A25R)  
    WATER (UNII: 059QF0KO0R)  
    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)  
    EDETATE DISODIUM (UNII: 7FLD91C86K)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    SACCHARIN SODIUM (UNII: SB8ZUX40TY)  
    DIMETHICONE (UNII: 92RU3N3Y1O)  
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
    SODIUM ALGINATE (UNII: C269C4G2ZQ)  
    SORBITOL (UNII: 506T60A25R)  
    WATER (UNII: 059QF0KO0R)  
    XANTHAN GUM (UNII: TTV12P4NEE)  
    Product Characteristics
    ColorgreenScore    
    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)  
    EDETATE DISODIUM (UNII: 7FLD91C86K)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    SACCHARIN SODIUM (UNII: SB8ZUX40TY)  
    DIMETHICONE (UNII: 92RU3N3Y1O)  
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
    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)
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