GAVISCON- aluminum hydroxide and magnesium carbonate liquid 
Haleon US Holdings LLC

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Drug Facts

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

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)

Directions (Extra Strength)

Other information (Regular Strength)

Other information (Extra Strength)

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

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

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

CHERRY

FLAVOR

12fl oz (355 ml)

©2014 GlaxoSmithKline

FRONT: 103698XA

BACK: 103699XA

Gavison Extra Strength Cherry 12 fl oz (355mL) label
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)

Revised: 4/2024
Document Id: 1546646a-c10a-0fbf-e063-6294a90a8f04
Set id: 2d74e5bc-1f10-4fb6-9258-cd906e360013
Version: 13
Effective Time: 20240404
 
Haleon US Holdings LLC