TUMS  ULTRA- calcium carbonate tablet, chewable 
Haleon US Holdings LLC

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Drug Facts

Active ingredient (in each tablet)

Calcium carbonate 1000 mg

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 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

Other information

Inactive ingredients

corn starch, crospovidone, dextrose, flavor, magnesium stearate, maltodextrin, sucrose, talc

Questions?

1-800-897-7535

Principal Display Panel

NDC 0135-0235-01

TUMS

CALCIUM CARBONATE

ANTACID

GOES TO WORK IN SECONDS!

Peppermint

ULTRASTRENGTH1000

72CHEWABLETABLETS

DO NOT USE IF PRINTED SEAL UNDER CAP IS TORN OR MISSING.

Dist. by: GSK CH,Warren, NJ 07059

©2021 GSK or licensor.

1001218 (Front Label)

1001219 (Back Label)

TUMS Ultra Peppermint 72 ct front label
TUMS   ULTRA
calcium carbonate tablet, chewable
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0135-0235
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CALCIUM CARBONATE (UNII: H0G9379FGK) (CARBONATE ION - UNII:7UJQ5OPE7D, CALCIUM CATION - UNII:2M83C4R6ZB) CALCIUM CARBONATE1000 mg
Inactive Ingredients
Ingredient NameStrength
CORN STARCH 3-E-DODECENYL SUCCINIC ANHYDRIDE MODIFIED (UNII: QG4MW19XYX)  
CROSPOVIDONE, UNSPECIFIED (UNII: 2S7830E561)  
DEXTROSE, UNSPECIFIED FORM (UNII: IY9XDZ35W2)  
MAGNESIUM STEARATE (UNII: 70097M6I30)  
MALTODEXTRIN (UNII: 7CVR7L4A2D)  
SUCROSE (UNII: C151H8M554)  
TALC (UNII: 7SEV7J4R1U)  
Product Characteristics
ColorwhiteScoreno score
ShapeROUNDSize19mm
FlavorPEPPERMINTImprint Code TUMS
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:0135-0235-0172 in 1 BOTTLE; Type 0: Not a Combination Product06/21/2021
2NDC:0135-0235-02160 in 1 BOTTLE; Type 0: Not a Combination Product07/23/2021
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM00106/21/2021
Labeler - Haleon US Holdings LLC (079944263)

Revised: 4/2024
Document Id: 154fd47f-f2c5-1e45-e063-6394a90a3125
Set id: 348d3dfa-6a52-4583-96e3-83c4bf2df45b
Version: 3
Effective Time: 20240404
 
Haleon US Holdings LLC