Gaviscon

aluminum hydroxide and magnesium carbonate · Liquid · Oral

Over the counter 3 recalls

Active ingredient

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

Purposes Antacid Antacid

Uses

Uses relieves heartburn acid indigestion sour stomach upset stomach associated with these symptoms

Warnings

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.

Ask a doctor or pharmacist

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

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

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

Directions

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

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

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?

Questions or comments? 1-800-452-0051

Label text from the FDA structured product label by Haleon US Holdings LLC (revised Feb 13, 2026). Long sections are shortened; the complete label is on DailyMed.

Active ingredients

Gaviscon NDC products (5)

NDCStrength & formLabelerType
0135-0094Aluminum Hydroxide 95 mg/15mL; Magnesium Carbonate 358 mg/15mL
Liquid
Haleon US Holdings LLCOTC MONOGRAPH DRUG
0135-0095Aluminum Hydroxide 254 mg/5mL; Magnesium Carbonate 237.5 mg/5mL
Liquid
Haleon US Holdings LLCOTC MONOGRAPH DRUG
0135-0098Aluminum Hydroxide 160 mg/1; Magnesium Carbonate 105 mg/1
Tablet, Chewable
Haleon US Holdings LLCOTC MONOGRAPH DRUG
0135-0430Aluminum Hydroxide 160 mg/1; Magnesium Carbonate 105 mg/1
Tablet, Chewable
Haleon US Holdings LLCOTC MONOGRAPH DRUG
0135-0574Aluminum Hydroxide 254 mg/5mL; Magnesium Carbonate 237.5 mg/5mL
Liquid
Haleon US Holdings LLCOTC MONOGRAPH DRUG

Gaviscon recalls

Frequently asked questions

What is Gaviscon used for?

Uses relieves heartburn acid indigestion sour stomach upset stomach associated with these symptoms

Who makes Gaviscon?

Gaviscon is listed by 1 labeler in the FDA NDC directory, including Haleon US Holdings LLC.

Has Gaviscon been recalled?

The FDA enforcement database lists 3 recalls for Gaviscon, most recently D-1322-2020 (class ii): Labeling: Label lacks warning - Magnesium safety warning is not present on the Gaviscon bottle label.