TUMS EXTRA STRENGTH, SMOOTHIES- calcium carbonate tablet, chewable 
GlaxoSmithKline Consumer Healthcare Holdings (US) LLC

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Drug Facts

Active ingredient (per tablet)

Calcium Carbonate 750 mg

Purpose

Antacid

Uses

relieves

•
heartburn
•
acid indigestion
•
sour stomach
•
upset stomach associated with these symptoms

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 10 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

•
adults and children 12 years of age and over: chew 2-4 tablets as symptoms occur, or as directed by a doctor. Chew or crush tablets completely before swallowing.
•
do not take for symptoms that persist for more than 2 weeks unless advised by a doctor

Other information

•
each tablet contains: elemental calcium 300 mg, magnesium 10 mg
•
store below 30oC (86oF). Keep the container tightly closed.

Inactive ingredients

corn starch, dextrose, flavor, magnesium stearate, maltodextrin, microcrystalline cellulose, sorbitol, sucrose, talc

Questions?

1-800-897-7535

Additional information

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

©2021 GSK group of companies or its licensor.

Dist. By:

GSK Consumer Healthcare

Warren, NJ 07059

Principal Display Panel

NDC 0135-1002-01

TUMS

CALCIUM CARBONATE

ANTACID

GOES TO WORK IN SECONDS!

Smoothies

Peppermint

SMOOTH DISSOLVE

140 CHEWABLE TABLETS

1001499 Front Label

1001500 Back Label

1001499 Tums Smoothies Peppermint 140 ct Front Label
TUMS  EXTRA STRENGTH, SMOOTHIES
calcium carbonate tablet, chewable
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0135-1002
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
STARCH, CORN (UNII: O8232NY3SJ)  
DEXTROSE, UNSPECIFIED FORM (UNII: IY9XDZ35W2)  
MAGNESIUM STEARATE (UNII: 70097M6I30)  
MALTODEXTRIN (UNII: 7CVR7L4A2D)  
MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)  
SORBITOL (UNII: 506T60A25R)  
SUCROSE (UNII: C151H8M554)  
TALC (UNII: 7SEV7J4R1U)  
Product Characteristics
ColorWHITEScoreno score
ShapeROUNDSize19mm
FlavorPEPPERMINTImprint Code TUMS;SD
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:0135-1002-01140 in 1 BOTTLE; Type 0: Not a Combination Product11/29/2021
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart33111/29/2021
Labeler - GlaxoSmithKline Consumer Healthcare Holdings (US) LLC (079944263)

Revised: 11/2021
Document Id: 11078d7c-373b-4c7b-b33b-f1deba613fc1
Set id: 11078d7c-373b-4c7b-b33b-f1deba613fc1
Version: 1
Effective Time: 20211129
 
GlaxoSmithKline Consumer Healthcare Holdings (US) LLC