TUMS CHEWY BITES- calcium carbonate tablet, chewable 
Haleon US Holdings LLC

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Drug Facts

Active ingredient (per tablet)

Calcium Carbonate USP 750mg

Purpose

Antacid

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

acacia gum, alcohol, ammonium hydroxide, beeswax, caprylic/capric triglycerides, carmine, carnauba wax, citric acid, coconut oil, corn starch, corn syrup, dextrin, ethyl acetate, ethyl alcohol, FD&C blue #1 alum lake, FD&C blue #2 alum lake, FD&C red #40, FD&C red #40 alum lake, FD&C yellow #5 alum lake (tartrazine), FD&C yellow #6, FD&C yellow #6 alum lake, flavors, gum arabic, isopropyl alcohol, maltodextrin, methyl paraben, modified corn starch, n-butyl alcohol, phosphoric acid, PVP, propyl paraben, propylene glycol, purified water, shellac, sodium benzoate, sorbic acid, sorbitol, soy bean oil, soy lecithin, sucrose, TBHQ, titanium dioxide, triacetin, vegetable oil

Questions?

Call 1-800-897-7535

Principal Display Panel

NDC 0135-0606-05

TUMS ®

CALCIUM CARBONATE

ANTACID

Chewy Bites

Assorted Berries

GOES TO WORK IN SECONDS!

EXTRA STRENGTH 750

54 CHEWABLE TABLETS

Safety sealed –

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

Distributed by:

GSKConsumer Healthcare

Warren, NJ 07059

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

©2020 GSK or licensor

Front Label: 1000948

Back Label: 1000949

1000948 Tums Chewy Bites 54ct es750
TUMS CHEWY BITES 
calcium carbonate tablet, chewable
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0135-0606
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
Inactive Ingredients
Ingredient NameStrength
ACACIA (UNII: 5C5403N26O)  
ALCOHOL (UNII: 3K9958V90M)  
AMMONIA (UNII: 5138Q19F1X)  
YELLOW WAX (UNII: 2ZA36H0S2V)  
MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)  
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. 5 (UNII: I753WB2F1M)  
FD&C YELLOW NO. 6 (UNII: H77VEI93A8)  
ISOPROPYL ALCOHOL (UNII: ND2M416302)  
MALTODEXTRIN (UNII: 7CVR7L4A2D)  
METHYLPARABEN (UNII: A2I8C7HI9T)  
MODIFIED CORN STARCH (1-OCTENYL SUCCINIC ANHYDRIDE) (UNII: 461P5CJN6T)  
BUTYL ALCOHOL (UNII: 8PJ61P6TS3)  
PHOSPHORIC ACID (UNII: E4GA8884NN)  
POVIDONE, UNSPECIFIED (UNII: FZ989GH94E)  
PROPYLPARABEN (UNII: Z8IX2SC1OH)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
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)  
TRIACETIN (UNII: XHX3C3X673)  
Product Characteristics
Colorred (red, pink, purple) Scoreno score
ShapeROUNDSize19mm
FlavorSTRAWBERRY (Assorted Berry: Strawberry, Raspberry, Mixed Berry) Imprint Code T
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:0135-0606-0132 in 1 BOTTLE; Type 0: Not a Combination Product03/01/2017
2NDC:0135-0606-0260 in 1 BOTTLE; Type 0: Not a Combination Product03/01/2017
3NDC:0135-0606-048 in 1 BOTTLE; Type 0: Not a Combination Product01/02/2020
4NDC:0135-0606-052 in 1 PACKAGE03/02/2021
454 in 1 BOTTLE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM00103/01/2017
Labeler - Haleon US Holdings LLC (079944263)

Revised: 4/2024
Document Id: 154f718b-ddba-fcad-e063-6394a90a9952
Set id: 72ac000c-90f7-42e2-88a6-740de114a954
Version: 8
Effective Time: 20240404
 
Haleon US Holdings LLC