TUMS ULTRA- calcium carbonate tablet, chewable

Tums by

Drug Labeling and Warnings

Tums by is a Otc medication manufactured, distributed, or labeled by GlaxoSmithKline Consumer Healthcare Holdings (US) LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient (per tablet)

Calcium carbonate 1000 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 7 tablets in 24 hours
• if pregnant do not take more than 5 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 2-3 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 400 mg, magnesium 10 mg
• store below 30°C (86°F)
• contains FD&C Yellow No. 5 (tartrazine) as a color additive

Inactive ingredients

corn starch, crospovidone, dextrose, FD&C red #40 lake, FD&C yellow #5 (tartrazine) lake, FD&C yellow #6 lake, flavor, magnesium stearate, maltodextrin, sucrose, talc

Questions?

1-800-897-7535

Additional Information

Safety sealed – Do not use if printed inner seal beneath cap is missing or broken.

Trademarks owned or licensed by GSK.
Dist. by: GSK CH
Warren, NJ 07059

©2022 GSK or licensor.

Gluten-Free

Principal Display Panel

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CALCIUM CARBONATE
TUMS
ANTACID

Tropical
Fruit

72 CHEWABLE TABLETS

ULTRA
STRENGTH 1000

202113 Back Label
202112 Front Label

INGREDIENTS AND APPEARANCE

TUMS  ULTRA
calcium carbonate tablet, chewable

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 0135-0553
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CALCIUM CARBONATE (UNII: H0G9379FGK) (CARBONATE ION - UNII:7UJQ5OPE7D, CALCIUM CATION - UNII:2M83C4R6ZB)	CALCIUM CARBONATE	1000 mg

Inactive Ingredients
Ingredient Name	Strength
STARCH, CORN (UNII: O8232NY3SJ)
CROSPOVIDONE, UNSPECIFIED (UNII: 2S7830E561)
DEXTROSE, UNSPECIFIED FORM (UNII: IY9XDZ35W2)
FD&C RED NO. 40 (UNII: WZB9127XOA)
ALUMINUM OXIDE (UNII: LMI26O6933)
FD&C YELLOW NO. 5 ALUMINUM LAKE (UNII: JQ6BLH9FR7)
FD&C YELLOW NO. 6 (UNII: H77VEI93A8)
MAGNESIUM STEARATE (UNII: 70097M6I30)
MALTODEXTRIN (UNII: 7CVR7L4A2D)
SUCROSE (UNII: C151H8M554)
TALC (UNII: 7SEV7J4R1U)

Product Characteristics
Color	WHITE (Off-white) , YELLOW, ORANGE, RED	Score	no score
Shape	ROUND	Size	19mm
Flavor	TROPICAL FRUIT PUNCH, STRAWBERRY (Strawberry-banana) , PINEAPPLE (Pineapple-orange) , ORANGE (Mandarin orange)	Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0135-0553-01	72 in 1 BOTTLE; Type 0: Not a Combination Product	03/01/2023

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M001	03/01/2023

Labeler - Haleon US Holdings LLC (079944263)