TUMS EXTRA STRENGTH, SMOOTHIES- calcium carbonate tablet, chewable

TUMS by

Drug Labeling and Warnings

TUMS by is a Otc medication manufactured, distributed, or labeled by Haleon US Holdings LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient (per tablet)

Calcium Carbonate 750 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 are

presently taking a prescription drug. Antacids may interact with certain prescription drugs.

When using this product

• do not take more than 10 tablets in 24 hours
• if pregnant do not take more than 6 tablets in 24 hours
• do not use the maximum dosage for more than 2 weeks except under the advice and supervision of a doctor

Keep out of reach of children.

Directions

• adults and children 12 years of age and over: chew 2-4 tablets as symptoms occur, or as directed by a doctor. Chew or crush tablets completely before swallowing.
• do not take for symptoms that persist for more than 2 weeks unless advised by a doctor

Other information

• each tablet contains: elemental calcium 300 mg, magnesium 10 mg
• store below 30oC (86oF). Keep the container tightly closed.

Inactive ingredients

corn starch, dextrose, flavor, magnesium stearate, maltodextrin, microcrystalline cellulose, sorbitol, sucrose, talc

Questions?

1-800-897-7535

Additional information

DO NOT USE IF PRINTED SEAL UNDER CAP IS TORN OR MISSING.

©2021 GSK group of companies or its licensor.

Dist. By:

GSK Consumer Healthcare

Warren, NJ 07059

Principal Display Panel

NDC: 0135-1002-01

TUMS

CALCIUM CARBONATE

ANTACID

GOES TO WORK IN SECONDS!

Smoothies

Peppermint

SMOOTH DISSOLVE

140 CHEWABLE TABLETS

1001499 Front Label

1001500 Back Label

INGREDIENTS AND APPEARANCE

TUMS  EXTRA STRENGTH, SMOOTHIES
calcium carbonate tablet, chewable

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 0135-1002
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CALCIUM CARBONATE (UNII: H0G9379FGK) (CALCIUM CATION - UNII:2M83C4R6ZB, CARBONATE ION - UNII:7UJQ5OPE7D)	CALCIUM CARBONATE	750 mg

Inactive Ingredients
Ingredient Name	Strength
STARCH, CORN (UNII: O8232NY3SJ)
DEXTROSE, UNSPECIFIED FORM (UNII: IY9XDZ35W2)
MAGNESIUM STEARATE (UNII: 70097M6I30)
MALTODEXTRIN (UNII: 7CVR7L4A2D)
MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)
SORBITOL (UNII: 506T60A25R)
SUCROSE (UNII: C151H8M554)
TALC (UNII: 7SEV7J4R1U)

Product Characteristics
Color	WHITE	Score	no score
Shape	ROUND	Size	19mm
Flavor	PEPPERMINT	Imprint Code	TUMS;SD
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0135-1002-01	140 in 1 BOTTLE; Type 0: Not a Combination Product	11/29/2021

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M001	11/29/2021

Labeler - Haleon US Holdings LLC (079944263)