GAVISCON - aluminum hydroxide and magnesium carbonate liquid 
GlaxoSmithKline Consumer Healthcare LP

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Drug Facts

Active ingredient (in each 15mL tablespoonful) Regular Strength

Aluminum hydroxide 95mg

Magnesium carbonate 358mg

Active ingredient (in each 5mL teaspoonful) Extra Strength

Aluminum hydroxide 254mg

Magnesium carbonate 237.5mg

Purpose

Antacid

Uses

relieves

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

Warnings

Do not use if you have kidney disease

Ask a doctor or pharmacist before use if you are

• taking a prescription drug. Antacids may interact with certain prescription drugs.
• if you are on a sodium-restricted diet

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
• 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
• 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 (15mL) contains: magnesium 115mg, sodium 52mg
• store at up to 25°C (77°F); avoid freezing
• keep tightly closed

Other information (Extra Strength)

• each teaspoon (5mL) contains: magnesium 80mg, sodium 14mg
• 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)

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

Questions or comments?

call toll-free (English/Spanish) 1-888-367-6471 weekdays

Distributed by:

GlaxoSmithKline Consumer Healthcare, L.P.

Moon Twp, PA 15108, Made in the U.S.A

©2010 GlaxoSmithKline

IMPORTANT:

Do not use if foil inner seal imprinted "SEALED FOR YOUR PROTECTION" is disturbed or missing.

Principal Display Panel

Gaviscon®

REGULAR STRENGTH

LIQUID ANTACID

• Fast-Acting

  Heartburn Relief

• Helps Keep Acid

  Down for Hours

COOL MINT

FLAVOR

12 fl oz (355 ml)

100631XA

Principal Display Panel

Gaviscon®

EXTRA STRENGTH

LIQUID ANTACID

• Fast-Acting

  Heartburn Relief

• Helps Keep Acid

  Down for Hours

COOL MINT

FLAVOR

12 fl oz (355 ml)

100651XA

GAVISCON  aluminum hydroxide and magnesium carbonate   liquid

Product Information Product Type HUMAN OTC DRUG NDC Product Code (Source) 0135-0094 Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALUMINUM HYDROXIDE (ALUMINUM HYDROXIDE) ALUMINUM HYDROXIDE 95 mg  in 15 mL MAGNESIUM CARBONATE (MAGNESIUM) MAGNESIUM CARBONATE 358 mg  in 15 mL

Inactive Ingredients Ingredient Name Strength BENZYL ALCOHOL   D&C YELLOW NO. 10   EDETATE DISODIUM   FD&C BLUE NO. 1   GLYCERIN   SACCHARIN SODIUM   SODIUM ALGINATE   SORBITOL   WATER   XANTHAN GUM

Product Characteristics Color GREEN Score      Shape Size Flavor MINT (cool mint) Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0135-0094-41 355 mL In 1 BOTTLE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part331	01/14/2011

GAVISCON  aluminum hydroxide and magnesium carbonate   liquid

Product Information Product Type HUMAN OTC DRUG NDC Product Code (Source) 0135-0095 Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALUMINUM HYDROXIDE (ALUMINUM HYDROXIDE) ALUMINUM HYDROXIDE 254 mg  in 5 mL MAGNESIUM CARBONATE (MAGNESIUM) MAGNESIUM CARBONATE 237.5 mg  in 5 mL

Inactive Ingredients Ingredient Name Strength BENZYL ALCOHOL   EDETATE DISODIUM   GLYCERIN   SACCHARIN SODIUM   DIMETHICONE   SILICON DIOXIDE   SODIUM ALGINATE   SORBITOL   WATER   XANTHAN GUM

Product Characteristics Color GREEN Score      Shape Size Flavor MINT (cool mint) Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0135-0095-41 355 mL In 1 BOTTLE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part331	01/14/2011

Labeler - GlaxoSmithKline Consumer Healthcare LP (828924212)

Revised: 02/2011GlaxoSmithKline Consumer Healthcare LP