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

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Drug Facts

Active ingredient (per tablet)

Calcium Carbonate USP 1000 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 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

•
adults and children 12 years of age and over: chew 2-3 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 400mg, sodium 2mg
•
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 ingredients (Assorted Tropical Fruit)

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

Inactive ingredients (Assorted Berry)

adipic acid, corn starch, FD&C blue #1 lake, FD&C red #40 lake, flavors, mineral oil, sodium polyphosphate, sucrose, talc

Inactive ingredient (Peppermint)

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

Inactive ingredients (Peppermint Tri-Color)

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

Questions?

1-800-897-7535weekdays

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

www.tums.com

GlaxoSmithKline

Moon Twp, PA 15108

Gluten-Free

Principal Display Panel

NDC 0135-0118-83

TUMS®

CALCIUM CARBONATE

ANTACID

ASSORTED FRUIT

ULTRA STRENGTH 1000

72 CHEWABLE TABLETS

GOES TO WORK IN SECONDS!

©2014 GSK

PAREVE

103662XA (Front Label)

103593XA (Back Label)

Tums Ultra Assorted Fruit 72 count front label

Principal Display Panel

NDC 0135-0180-02

TUMS®

CALCIUM CARBONATE

ANTACID

TROPICAL FRUIT

ULTRA STRENGTH 1000

72 CHEWABLE TABLETS

GOES TO WORK IN SECONDS!

©2014 GSK

PAREVE

103634XA (Front Label)

103591XA (Back Label)

Tums Ultra Tropical Fruit 72 count front label

Principal Display Panel

NDC 0135-0181-02

TUMS®

CALCIUM CARBONATE

ANTACID

ASSORTED BERRIES

ULTRA STRENGTH 1000

72 CHEWABLE TABLETS

GOES TO WORK IN SECONDS!

©2014 GSK

PAREVE

103665XA (Front Label)

103588XA (Back Label)

Tums Ultra Assorted Berries 72 count front label

Principal Display Panel

NDC 0135-0228-06

TUMS®

CALCIUM CARBONATE

ANTACID

PEPPERMINT

ULTRA STRENGTH 1000

72 CHEWABLE TABLETS

GOES TO WORK IN SECONDS!

©2014 GSK

103664XA (Front Label)

103592XA (Back Label)

Tums Ultra Peppermint 72 count front label

Principal Display Panel

NDC 0135-0540-01

TUMS®

ANTACID

CALICUM CARBONATE

PEPPERMINT

ULTRA STRENGTH 1000

86 CHEWABLE TABLETS

20% MORE FREE

PAREVE

©2014 GSK

104475XA (Front Label)

104476XA (Back Label)

Tums Ultra tricolor Peppermint 86 ct label
TUMS  ULTRA
calcium carbonate tablet, chewable
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0135-0118
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
SUCROSE (UNII: C151H8M554)  
STARCH, CORN (UNII: O8232NY3SJ)  
TALC (UNII: 7SEV7J4R1U)  
MINERAL OIL (UNII: T5L8T28FGP)  
ADIPIC ACID (UNII: 76A0JE0FKJ)  
SODIUM POLYMETAPHOSPHATE (UNII: P1BM4ZH95L)  
FD&C RED NO. 40 (UNII: WZB9127XOA)  
FD&C YELLOW NO. 6 (UNII: H77VEI93A8)  
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
ALUMINUM OXIDE (UNII: LMI26O6933)  
Product Characteristics
ColorPINK (orange, yellow, green) Scoreno score
ShapeROUNDSize19mm
FlavorCHERRY (assorted fruit, orange, lemon, lime) Imprint Code TUMS
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:0135-0118-0186 in 1 BOTTLE; Type 0: Not a Combination Product02/12/2010
2NDC:0135-0118-04265 in 1 BOTTLE; Type 0: Not a Combination Product02/12/2010
3NDC:0135-0118-14160 in 1 BOTTLE; Type 0: Not a Combination Product02/12/2010
4NDC:0135-0118-8372 in 1 BOTTLE; Type 0: Not a Combination Product02/12/2010
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM00102/12/2010
TUMS  ULTRA
calcium carbonate tablet, chewable
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0135-0180
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
SUCROSE (UNII: C151H8M554)  
STARCH, CORN (UNII: O8232NY3SJ)  
TALC (UNII: 7SEV7J4R1U)  
MINERAL OIL (UNII: T5L8T28FGP)  
SODIUM POLYMETAPHOSPHATE (UNII: P1BM4ZH95L)  
FD&C RED NO. 40 (UNII: WZB9127XOA)  
FD&C YELLOW NO. 6 (UNII: H77VEI93A8)  
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
ALUMINUM OXIDE (UNII: LMI26O6933)  
Product Characteristics
ColorORANGE (red-orange, cream to off-white, light yellow) Scoreno score
ShapeROUNDSize19mm
FlavorTROPICAL FRUIT PUNCH (assorted tropical fruit, mandarin orange, orange-pineapple, strawberry-banana) Imprint Code TUMS
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:0135-0180-0186 in 1 BOTTLE; Type 0: Not a Combination Product02/12/2010
2NDC:0135-0180-0272 in 1 BOTTLE; Type 0: Not a Combination Product02/12/2010
3NDC:0135-0180-14160 in 1 BOTTLE; Type 0: Not a Combination Product02/12/2010
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM00102/12/2010
TUMS  ULTRA
calcium carbonate tablet, chewable
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0135-0181
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
SUCROSE (UNII: C151H8M554)  
STARCH, CORN (UNII: O8232NY3SJ)  
TALC (UNII: 7SEV7J4R1U)  
MINERAL OIL (UNII: T5L8T28FGP)  
ADIPIC ACID (UNII: 76A0JE0FKJ)  
SODIUM POLYMETAPHOSPHATE (UNII: P1BM4ZH95L)  
FD&C RED NO. 40 (UNII: WZB9127XOA)  
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
ALUMINUM OXIDE (UNII: LMI26O6933)  
Product Characteristics
ColorPINK (mauve, bluish) Scoreno score
ShapeROUNDSize19mm
FlavorBERRY (assorted berry, strawberry, raspberry, mixed berry) Imprint Code TUMS
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:0135-0181-013 in 1 CARTON02/12/2010
112 in 1 PACKAGE; Type 0: Not a Combination Product
2NDC:0135-0181-0272 in 1 BOTTLE; Type 0: Not a Combination Product02/12/2010
3NDC:0135-0181-0312 in 1 PACKAGE; Type 0: Not a Combination Product02/12/2010
4NDC:0135-0181-05265 in 1 BOTTLE; Type 0: Not a Combination Product02/12/2010
5NDC:0135-0181-0686 in 1 BOTTLE; Type 0: Not a Combination Product02/12/2010
6NDC:0135-0181-071 in 1 CARTON02/12/2010
612 in 1 PACKAGE; Type 0: Not a Combination Product
7NDC:0135-0181-14160 in 1 BOTTLE; Type 0: Not a Combination Product02/12/2010
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM00102/12/2010
TUMS  ULTRA
calcium carbonate tablet, chewable
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0135-0228
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
SUCROSE (UNII: C151H8M554)  
STARCH, CORN (UNII: O8232NY3SJ)  
TALC (UNII: 7SEV7J4R1U)  
MINERAL OIL (UNII: T5L8T28FGP)  
SODIUM POLYMETAPHOSPHATE (UNII: P1BM4ZH95L)  
Product Characteristics
ColorWHITEScoreno score
ShapeROUNDSize19mm
FlavorPEPPERMINTImprint Code TUMS
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:0135-0228-0112 in 1 PACKAGE; Type 0: Not a Combination Product02/12/2010
2NDC:0135-0228-0410 in 1 PACKAGE; Type 0: Not a Combination Product02/12/2010
3NDC:0135-0228-05160 in 1 BOTTLE; Type 0: Not a Combination Product02/12/2010
4NDC:0135-0228-0672 in 1 BOTTLE; Type 0: Not a Combination Product02/12/2010
5NDC:0135-0228-0786 in 1 BOTTLE; Type 0: Not a Combination Product02/10/201504/30/2018
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM00102/12/2010
TUMS  ULTRA
calcium carbonate tablet, chewable
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0135-0540
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
SUCROSE (UNII: C151H8M554)  
STARCH, CORN (UNII: O8232NY3SJ)  
TALC (UNII: 7SEV7J4R1U)  
MINERAL OIL (UNII: T5L8T28FGP)  
SODIUM POLYMETAPHOSPHATE (UNII: P1BM4ZH95L)  
FD&C RED NO. 40 (UNII: WZB9127XOA)  
ALUMINUM OXIDE (UNII: LMI26O6933)  
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
Product Characteristics
ColorWHITE, RED, GREENScoreno score
ShapeROUNDSize19mm
FlavorPEPPERMINTImprint Code TUMS
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:0135-0540-0186 in 1 BOTTLE; Type 0: Not a Combination Product02/12/2010
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM00102/12/2010
Labeler - Haleon US Holdings LLC (079944263)

Revised: 2/2024
Document Id: 09be49e9-b102-4c0a-9501-46b457400c29
Set id: f4786707-a0f7-4ba8-9656-06278d1b4b6c
Version: 16
Effective Time: 20240214
 
Haleon US Holdings LLC