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GAVISCON

GlaxoSmithKline Consumer Healthcare LP

Drug Facts


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Aluminum hydroxide 95mg

Magnesium carbonate 358mg

Aluminum hydroxide 254mg

Magnesium carbonate 237.5mg

Antacid

relieves

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

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.

  • •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
  • •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
  • each tablespoon (15mL) contains: magnesium 115mg, sodium 52mg
  • •store at up to 25°C (77°F); avoid freezing
  • •keep tightly closed
  • each teaspoon (5mL) contains: magnesium 80mg, sodium 14mg
  • •store at up to 25°C (77°F); avoid freezing
  • •keep tightly closed

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

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

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

NDC 0135-0094-41

Gaviscon®

REGULAR STRENGTH

LIQUID ANTACID

  • Fast-Acting

    Heartburn Relief

  • Helps Keep Acid

    Down for Hours

COOL MINT

FLAVOR

12 fl oz (355 ml)

100631XB

Principal Display Panel

NDC 0135-0095-41

Gaviscon®

EXTRA STRENGTH

LIQUID ANTACID

  • Fast-Acting

    Heartburn Relief

  • Helps Keep Acid

    Down for Hours

COOL MINT

FLAVOR

12 fl oz (355 ml)

100651XB

GAVISCON

aluminum hydroxide and magnesium carbonate LIQUID

Product Information

Product Type Human otc drug label Item Code (Source) NDC:0135-0094
Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
aluminum hydroxide 95 mg
MAGNESIUM CARBONATE 358 mg

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

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:0135-0094-41 355 in 1 BOTTLE
2 NDC:0135-0094-42 177 in 1 BOTTLE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part331 2011-01-14


GAVISCON

aluminum hydroxide and magnesium carbonate LIQUID

Product Information

Product Type Human otc drug label Item Code (Source) NDC:0135-0095
Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
aluminum hydroxide 254 mg
MAGNESIUM CARBONATE 237.5 mg

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

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:0135-0095-41 355 in 1 BOTTLE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part331 2011-01-14


PLEASE, BE CAREFUL!
Be sure to consult your doctor before taking any medication!
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