TUMS CHEWY BITES- calcium carbonate tablet, chewable 
Select Consumer Group

----------

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, beeswax, carmine, carnauba wax, citric acid, coconut oil, corn starch, corn syrup, dextrin, FD&C blue no. 2 aluminum lake, FD&C red no. 40, FD&C red no. 40 aluminum lake, FD&C yellow no. 5 aluminum lake (tartrazine), maltodextrin, medium chain triglycerides, methylparaben, natural and artificial flavors, pharmaceutical ink, phosphoric acid, povidone, propylene glycol, propylparaben, purified water, shellac, sodium benzoate, sorbic acid, sorbitol, soy lecithin, sucrose, titanium dioxide, triacetin, vegetable oil

Inactive ingredients

Questions or comments?

1-800-897-7535

Generic Section (Bottles)

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

Generic Section (2 ct. Pouch)

Safety sealed – Do not use if pouch is open or torn.

Principal Display Panel (108 ct. Bottle)

GOES TO WORK IN SECONDS!

CALCIUM CARBONATE

TUMS

ANTACID

Chewy Bites

Assorted Berries

EXTRA STRENGTH 750

108 CHEWABLE TABLETS

Tums Chewy Bites Asst Berries 108 Tablets
TUMS CHEWY BITES 
calcium carbonate tablet, chewable
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:85237-1860(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)  
STARCH, WHEAT (UNII: 79QS2MG2LP)  
ETHYL ACETATE (UNII: 76845O8NMZ)  
FD&C BLUE NO. 1 ALUMINUM LAKE (UNII: J9EQA3S2JM)  
FD&C BLUE NO. 2 ALUMINUM LAKE (UNII: 4AQJ3LG584)  
FD&C RED NO. 40 (UNII: WZB9127XOA)  
FD&C RED NO. 40 ALUMINUM LAKE (UNII: 6T47AS764T)  
FD&C YELLOW NO. 5 ALUMINUM LAKE (UNII: JQ6BLH9FR7)  
FD&C YELLOW NO. 6 (UNII: H77VEI93A8)  
FD&C YELLOW NO. 6 ALUMINUM LAKE (UNII: GYP6Z2JR6Q)  
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)  
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 (UNII: L7HT8F1ZOD)  
SOYBEAN LECITHIN (UNII: 1DI56QDM62)  
SUCROSE (UNII: C151H8M554)  
TERT-BUTYLHYDROQUINONE (UNII: C12674942B)  
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
TRIACETIN (UNII: XHX3C3X673)  
CORN OIL (UNII: 8470G57WFM)  
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:85237-1860-120 in 1 BOX, UNIT-DOSE03/01/2017
12 in 1 POUCH; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM00103/01/2017
Labeler - Select Consumer Group (119185084)
Registrant - Select Consumer Group (119185084)
Establishment
NameAddressID/FEIBusiness Operations
Select Consumer Group119185084repack(85237-1860)

Revised: 8/2025
Document Id: 3ca9f07f-cea6-7805-e063-6394a90a18b2
Set id: 3caa037e-3424-f9ce-e063-6294a90ac1e8
Version: 2
Effective Time: 20250818
 
Select Consumer Group