TUMS- calcium carbonate tablet 
Haleon US Holdings LLC

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Drug Facts

Active ingredient (per tablet)

Calcium Carbonate USP 500 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

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.

Directions

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

Other information

•
each tablet contains: elemental calcium 200mg
•
store below 30oC (86oF)

Inactive ingredients (assorted fruit)

Adipic acid, corn starch, FD&C blue #1 lake, FD&C red #40 lake, FD&C yellow #5 (tartrazine) lake, FD&C yellow #6 lake, flavors, mineral oil, sodium polyphosphate, sucrose, talc

Inactive ingredient (peppermint)

corn starch, flavor, mineral oil, sodium polyphosphate, sucrose, talc

Questions?

1-800-897-7535

weekdays

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

Gluten-Free

www.tums.com

GlaxoSmithKline

Moon Twp, PA 15108

PRINCIPAL DISPLAY PANEL

NDC 0135-0071-27

TUMS®

CALCIUM CARBONATE

ANTACID

REGULAR STRENGTH 500

Goes to Work in Seconds!

Assorted Fruit

150 CHEWABLE TABLETS

PAREVE

©2014 GSK

Front Label: 103784XA

Back Label: 103783XA

Tums Regular Assorted Fruit 150 count label

Principal Display Panel

NDC 0135-0070-27

TUMS®

CALCIUM CARBONATE

ANTACID

REGULAR STRENGTH 500

Goes to Work in Seconds!

Peppermint

150 CHEWABLE TABLETS

PAREVE

©2014 GSK

Front Label: 103781XA

Back Label: 103780XA

Tums Regular Peppermint 150 count label
TUMS 
calcium carbonate tablet
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0135-0071
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
ADIPIC ACID (UNII: 76A0JE0FKJ)  
STARCH, CORN (UNII: O8232NY3SJ)  
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
FD&C RED NO. 40 (UNII: WZB9127XOA)  
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
FD&C YELLOW NO. 6 (UNII: H77VEI93A8)  
MINERAL OIL (UNII: T5L8T28FGP)  
SODIUM POLYMETAPHOSPHATE (UNII: P1BM4ZH95L)  
SUCROSE (UNII: C151H8M554)  
TALC (UNII: 7SEV7J4R1U)  
Product Characteristics
ColorPINK (orange, yellow, green) Scoreno score
ShapeROUNDSize16mm
FlavorCHERRY (assorted fruit, orange, lemon, lime) Imprint Code TUMS
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:0135-0071-27150 in 1 BOTTLE; Type 0: Not a Combination Product03/10/2010
2NDC:0135-0071-4812 in 1 PACKAGE; Type 0: Not a Combination Product03/10/2010
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM00103/10/2010
TUMS 
calcium carbonate tablet
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0135-0070
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
STARCH, CORN (UNII: O8232NY3SJ)  
MINERAL OIL (UNII: T5L8T28FGP)  
SODIUM POLYMETAPHOSPHATE (UNII: P1BM4ZH95L)  
SUCROSE (UNII: C151H8M554)  
TALC (UNII: 7SEV7J4R1U)  
Product Characteristics
ColorWHITEScoreno score
ShapeROUNDSize16mm
FlavorPEPPERMINTImprint Code TUMS
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:0135-0070-033 in 1 CELLO PACK03/10/2010
112 in 1 PACKAGE; Type 0: Not a Combination Product
2NDC:0135-0070-27150 in 1 BOTTLE; Type 0: Not a Combination Product03/10/2010
3NDC:0135-0070-4812 in 1 PACKAGE; Type 0: Not a Combination Product03/10/2010
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM00103/10/2010
Labeler - Haleon US Holdings LLC (079944263)

Revised: 3/2024
Document Id: b826d33d-fb25-442b-8ffa-172acf2b4780
Set id: 35f79dcf-1743-4d9f-aba5-5ead6b056309
Version: 12
Effective Time: 20240315
 
Haleon US Holdings LLC