TUMS  REGULAR STRENGTH- calcium carbonate tablet, chewable 
Haleon US Holdings LLC

----------

Drug Facts

Active ingredient (per tablet)

Calcium Carbonate USP 500mg

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 15 tablets in 24 hours
  • if pregnant do not take more than 10 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.

Click here to enter Precautions

Directions

Other information

Inactive ingredients

cellulose, dextrose, flavor, maltodextrin, mineral oil, polyethylene glycol, talc

Questions?

1-800-897-7535

Principal Display Panel

NDC 0135-0611-01

TUMS ®

ANTACID

CALCIUM CARBONATE

GOES TO WORK IN SECONDS!

Mint

REGULARE STRENGTH 500

150 CHEWABLE TABLETS

PAREVE

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

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

Dist. by:

GSKConsumer Healthcare

Warren, NJ 07059

©2014 GSK or its licensor

Front Label: 105436XA

Back Label: 105437XA

Tums Regular Mint 150 ct front label
TUMS   REGULAR STRENGTH
calcium carbonate tablet, chewable
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0135-0611
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CALCIUM CARBONATE (UNII: H0G9379FGK) (CALCIUM CATION - UNII:2M83C4R6ZB, CARBONATE ION - UNII:7UJQ5OPE7D) CALCIUM CARBONATE500 mg
Inactive Ingredients
Ingredient NameStrength
POWDERED CELLULOSE (UNII: SMD1X3XO9M)  
DEXTROSE, UNSPECIFIED FORM (UNII: IY9XDZ35W2)  
MALTODEXTRIN (UNII: 7CVR7L4A2D)  
MINERAL OIL (UNII: T5L8T28FGP)  
POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)  
TALC (UNII: 7SEV7J4R1U)  
Product Characteristics
ColorwhiteScoreno score
ShapeROUNDSize16mm
FlavorPEPPERMINTImprint Code TUMS
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:0135-0611-01150 in 1 BOTTLE; Type 0: Not a Combination Product09/01/2016
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM00109/01/2016
Labeler - Haleon US Holdings LLC (079944263)

Revised: 3/2024
Document Id: 12c98e11-49eb-b55e-e063-6394a90ae122
Set id: ac80f627-3f51-425b-8c75-e07363048b00
Version: 5
Effective Time: 20240303
 
Haleon US Holdings LLC