TUMS CHEWY BITES BERRY SHAKE- calcium carbonate tablet, chewable

Tums Chewy Bites by

Drug Labeling and Warnings

Tums Chewy Bites 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 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 6 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 chewable tablet contains:elemental calcium 305 mg
• do not store above 25°C (77°F)

Inactive ingredients

Acacia gum, alcohol, ammonium hydroxide, beeswax, carmine, carnauba wax, citric acid, coconut oil, corn starch, corn syrup, dextrin, ethyl acetate, ethyl alcohol, FD&C blue no. 1 aluminum lake, FD&C blue no. 2 aluminum lake, FD&C red no. 40 aluminum lake, FD&C yellow no. 6 aluminum lake, flavors, gum arabic, isopropyl alcohol, maltodextrin, methyl paraben, n-butyl alcohol, phosphoric acid, propylene glycol, propylparaben, purified water, shellac, sorbic acid, sorbitol, soybean oil, soy lecithin, sucrose, tertiary butylhydroquinone, titanium dioxide, vegetable oil

Questions or comments?

Call 1-800-897-7535

Principal Display Panel

NDC: 0135-0184-01

TUMS

CALCIUM CARBONATE

ANTACID

Chewy Bites

Berry Shake

GOES TO WORK IN SECONDS!

EXTRA STRENGTH 750

32 CHEWABLE TABLETS

Safety sealed –

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

Distributed by:

GSK Consumer Healthcare

Warren, NJ 07059

Trademarks are owned by or licensed to the GSK group of companies.

©2020 GSK or licensor.

Front Label: 1001083

Back Label: 1001084

INGREDIENTS AND APPEARANCE

TUMS CHEWY BITES   BERRY SHAKE
calcium carbonate tablet, chewable

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 0135-0184
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
ACACIA (UNII: 5C5403N26O)
ALCOHOL (UNII: 3K9958V90M)
AMMONIA (UNII: 5138Q19F1X)
YELLOW WAX (UNII: 2ZA36H0S2V)
CARMINIC ACID (UNII: CID8Z8N95N)
CARNAUBA WAX (UNII: R12CBM0EIZ)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
COCONUT OIL (UNII: Q9L0O73W7L)
STARCH, CORN (UNII: O8232NY3SJ)
CORN SYRUP (UNII: 9G5L16BK6N)
ICODEXTRIN (UNII: 2NX48Z0A9G)
ETHYL ACETATE (UNII: 76845O8NMZ)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
ALUMINUM OXIDE (UNII: LMI26O6933)
FD&C BLUE NO. 2 (UNII: L06K8R7DQK)
FD&C RED NO. 40 (UNII: WZB9127XOA)
FD&C YELLOW NO. 6 (UNII: H77VEI93A8)
ISOPROPYL ALCOHOL (UNII: ND2M416302)
MALTODEXTRIN (UNII: 7CVR7L4A2D)
METHYLPARABEN (UNII: A2I8C7HI9T)
BUTYL ALCOHOL (UNII: 8PJ61P6TS3)
PHOSPHORIC ACID (UNII: E4GA8884NN)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
PROPYLPARABEN (UNII: Z8IX2SC1OH)
WATER (UNII: 059QF0KO0R)
SHELLAC (UNII: 46N107B71O)
SORBIC ACID (UNII: X045WJ989B)
SORBITOL (UNII: 506T60A25R)
SOYBEAN OIL (UNII: 241ATL177A)
LECITHIN, SOYBEAN (UNII: 1DI56QDM62)
SUCROSE (UNII: C151H8M554)
TERT-BUTYLHYDROQUINONE (UNII: C12674942B)
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
CORN OIL (UNII: 8470G57WFM)

Product Characteristics
Color	pink	Score	no score
Shape	ROUND	Size	19mm
Flavor	BERRY (Shake)	Imprint Code	T
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0135-0184-01	1 in 1 CARTON	07/01/2021
1		32 in 1 BOTTLE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M001	03/05/2021

Labeler - Haleon US Holdings LLC (079944263)