TUMS NATURALS- calcium carbonate tablet, chewable

Tums by

Drug Labeling and Warnings

Tums by is a Otc medication manufactured, distributed, or labeled by Haleon US Holdings LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient (per tablet)

Calcium carbonate 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. 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 400 mg
• do not store above 25°C (77°F)

Inactive ingredients (Black Cherry & Watermelon)

calcium stearate, carmine, dextrose, flavors, gum arabic

Inactive ingredients (Coconut Pineapple)

calcium stearate, dextrose, flavor, gum arabic

Questions or comments?

1-800-897-7535

Generic Section

Do not use if printed inner safety seal under cap is broken or missing.

Gluten-Free

Non-GMO

Principal Display Panel (Black Cherry & Watermelon)

GOES TO WORK IN SECONDS!

CALCIUM CARBONATE

TUMS

ANTACID

Naturals

NOARTIFICIAL FLAVORS OR DYES

Black Cherry & Watermelon

ULTRA STRENGTH 1000

56 CHEWABLE TABLETS

Principal Display Panel (Coconut Pineapple)

gsk

GOES TO WORK IN SECONDS!

CALCIUM CARBONATE

TUMS

ANTACID

NEW

Naturals

NO ARTIFICIAL FLAVORS OR DYES

Coconut Pineapple

ULTRA STRENGTH 1000

56 CHEWABLE TABLETS

INGREDIENTS AND APPEARANCE

TUMS  NATURALS
calcium carbonate tablet, chewable

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 0135-1326
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CALCIUM CARBONATE (UNII: H0G9379FGK) (CALCIUM CATION - UNII:2M83C4R6ZB, CARBONATE ION - UNII:7UJQ5OPE7D)	CALCIUM CARBONATE	1000 mg

Inactive Ingredients
Ingredient Name	Strength
CALCIUM STEARATE (UNII: 776XM7047L)
DEXTROSE, UNSPECIFIED FORM (UNII: IY9XDZ35W2)
ACACIA (UNII: 5C5403N26O)

Product Characteristics
Color	PINK (Reddish-pink) , PINK (Light pink)	Score	no score
Shape	ROUND	Size	16mm
Flavor	CHERRY (Black Cherry) , WATERMELON	Imprint Code	TUMS;N
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0135-1326-01	56 in 1 BOTTLE; Type 0: Not a Combination Product	10/15/2020
2	NDC: 0135-1326-03	190 in 1 BOTTLE; Type 0: Not a Combination Product	10/15/2020
3	NDC: 0135-1326-02	10 in 1 BOTTLE; Type 0: Not a Combination Product	03/12/2021
4	NDC: 0135-1326-05	2 in 1 POUCH; Type 0: Not a Combination Product	06/10/2021

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M001	10/15/2020

TUMS  NATURALS
calcium carbonate tablet, chewable

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 0135-1328
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CALCIUM CARBONATE (UNII: H0G9379FGK) (CALCIUM CATION - UNII:2M83C4R6ZB, CARBONATE ION - UNII:7UJQ5OPE7D)	CALCIUM CARBONATE	1000 mg

Inactive Ingredients
Ingredient Name	Strength
CALCIUM STEARATE (UNII: 776XM7047L)
DEXTROSE, UNSPECIFIED FORM (UNII: IY9XDZ35W2)
ACACIA (UNII: 5C5403N26O)

Product Characteristics
Color	WHITE	Score	no score
Shape	ROUND	Size	16mm
Flavor	COCONUT, PINEAPPLE	Imprint Code	TUMS;N
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0135-1328-01	56 in 1 BOTTLE; Type 0: Not a Combination Product	10/15/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M001	10/15/2020

Labeler - Haleon US Holdings LLC (079944263)