TUMS CHEWY BITES WITH GAS RELIEF- calcium carbonate and simethicone tablet, chewable 
Haleon US Holdings LLC

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Drug Facts

Active ingredients (per tablet)

Calcium Carbonate USP 750 mg

Simethicone USP 80 mg

Purposes

Antacid

Antigas

Uses

relieves

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

Other information

Inactive ingredients

alcohol, ammonium hydroxide, beeswax, carnauba wax, citric acid, coconut oil, corn starch, corn syrup, dextrin, ethyl acetate, ethyl alcohol, FD&C blue #1 alum lake, FD&C Red#40, FD&C red #40 alum lake, FD&C yellow #5 alum lake (tartrazine), FD&C yellow #6 alum lake, flavors, gum arabic, isopropyl alcohol, maltodextrin, medium-chain triglycerides, methylparaben, modified corn starch, n-butyl alcohol, phosphoric acid, propylene glycol, propylparaben, purified water, shellac, sodium benzoate, sorbic acid, sorbitol, soy bean oil, soy lecithin, sucrose, tert-butylhydroquinone, titanium dioxide, vegetable oil

Questions or comments?

Call toll-free 1-800-897-7535

Additional Information

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

Dist. by:

GSKConsumer Healthcare

Warren, NJ 07059

©2022 GSK or its licensor.

Trademarks owned or licensed by GSK.

Principal Display Panel

NEW LOOK

TUMS + Gas Relief

ANTACID/ANTIGAS

FAST RELIEF OF HEARTBURN & GAS

CALCIUM CARBONATE / SIMETHICONE

Helps relieve heartburn and gas, bloating and discomfort

Lemon & Strawberry

54 CHEWABLE TABLETS

201339 Front Label

Tums + GasRelief Lemon and Strawberry 54 ct
TUMS CHEWY BITES WITH GAS RELIEF 
calcium carbonate and simethicone tablet, chewable
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0135-0624
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CALCIUM CARBONATE (UNII: H0G9379FGK) (CALCIUM CATION - UNII:2M83C4R6ZB, CARBONATE ION - UNII:7UJQ5OPE7D) CALCIUM CARBONATE750 mg
DIMETHICONE (UNII: 92RU3N3Y1O) (DIMETHICONE - UNII:92RU3N3Y1O) DIMETHICONE80 mg
Inactive Ingredients
Ingredient NameStrength
ALCOHOL (UNII: 3K9958V90M)  
AMMONIA (UNII: 5138Q19F1X)  
YELLOW WAX (UNII: 2ZA36H0S2V)  
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 ALUMINUM LAKE (UNII: J9EQA3S2JM)  
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)  
ACACIA (UNII: 5C5403N26O)  
ISOPROPYL ALCOHOL (UNII: ND2M416302)  
MALTODEXTRIN (UNII: 7CVR7L4A2D)  
MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)  
METHYLPARABEN (UNII: A2I8C7HI9T)  
MODIFIED CORN STARCH (1-OCTENYL SUCCINIC ANHYDRIDE) (UNII: 461P5CJN6T)  
BUTYL ALCOHOL (UNII: 8PJ61P6TS3)  
PHOSPHORIC ACID (UNII: E4GA8884NN)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
PROPYLPARABEN (UNII: Z8IX2SC1OH)  
WATER (UNII: 059QF0KO0R)  
SHELLAC (UNII: 46N107B71O)  
SODIUM BENZOATE (UNII: OJ245FE5EU)  
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
Colorred (red, yellow) Scoreno score
ShapeROUNDSize19mm
FlavorSTRAWBERRY (Strawberry, Lemon) Imprint Code T
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:0135-0624-0128 in 1 BOTTLE; Type 0: Not a Combination Product03/01/2018
2NDC:0135-0624-0254 in 1 BOTTLE; Type 0: Not a Combination Product03/01/2019
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM00103/01/2018
Labeler - Haleon US Holdings LLC (079944263)

Revised: 3/2024
Document Id: 12b8887d-92b9-d88f-e063-6294a90a6da8
Set id: 6d7be7e4-4bff-4cfd-bbbe-df412ac9db10
Version: 8
Effective Time: 20240302
 
Haleon US Holdings LLC