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NDC 00135-0610-02 TUMS 1000 mg/1 Details

TUMS 1000 mg/1

TUMS is a ORAL TABLET, CHEWABLE in the HUMAN OTC DRUG category. It is labeled and distributed by GlaxoSmithKline Consumer Healthcare Holdings (US) LLC. The primary component is CALCIUM CARBONATE.

MedlinePlus Drug Summary

Calcium carbonate is a dietary supplement used when the amount of calcium taken in the diet is not enough. Calcium is needed by the body for healthy bones, muscles, nervous system, and heart. Calcium carbonate also is used as an antacid to relieve heartburn, acid indigestion, and upset stomach. It is available with or without a prescription. This medication is sometimes prescribed for other uses; ask your doctor or pharmacist for more information.

Related Packages: 00135-0610-02
Last Updated: 11/30/2022
MedLinePlus Full Drug Details: Calcium Carbonate

Product Information

NDC	00135-0610
Product ID	0135-0610_23419246-72a9-4295-805d-4eb4eeab0327
Associated GPIs
GCN Sequence Number	n/a
GCN Sequence Number Description	n/a
HIC3	n/a
HIC3 Description	n/a
GCN	n/a
HICL Sequence Number	n/a
HICL Sequence Number Description	n/a
Brand/Generic	n/a
Proprietary Name	TUMS
Proprietary Name Suffix	ULTRA
Non-Proprietary Name	calcium carbonate
Product Type	HUMAN OTC DRUG
Dosage Form	TABLET, CHEWABLE
Route	ORAL
Active Ingredient Strength	1000
Active Ingredient Units	mg/1
Substance Name	CALCIUM CARBONATE
Labeler Name	GlaxoSmithKline Consumer Healthcare Holdings (US) LLC
Pharmaceutical Class	n/a
DEA Schedule	n/a
Marketing Category	OTC MONOGRAPH FINAL
Application Number	part331
Listing Certified Through	2022-12-31

Package

Package Images

NDC 00135-0610-02 (00135061002)

Pricing Information	N/A
NDC Package Code	0135-0610-02
Billing NDC	00135061002
Package	160 TABLET, CHEWABLE in 1 BOTTLE (0135-0610-02)
Marketing Start Date	2016-09-01
NDC Exclude Flag	N

Standard Product Labeling (SPL)/Prescribing Information SPL ee3faeab-4cea-4852-9ddf-901a346c092a Details

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 chewable tablet contains: elemental calcium 400mg
•: do not store below 25oC (77oF)

Inactive ingredients (Tropical Fruit)

cellulose, dextrose, FD&C red #40 alum lake, FD&C yellow #5 alum lake (tartrazine), FD&C yellow #6 alum lake, flavor, maltodextrin, mineral oil, polyethylene glycol, talc

Inactive ingredient (Mint)

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

Questions?

1-800-897-7535

Principal Display Panel

NDC 0135-0610-01

TUMS®

CALCIUM CARBONATE

ANTACID

GOES TO WORK IN SECONDS!

TROPICAL FRUIT

ULTRA STRENGTH 1000

72 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:

GSK Consumer Healthcare

Warren, NJ 07059

105439XA (Front Label)

105440XA (Back Label)

Tums Ultra Tropical Fruit 72 count front label

Principal Display Panel

NDC 0135-0612-01

TUMS®

CALCIUM CARBONATE

ANTACID

GOES TO WORK IN SECONDS!

MINT

ULTRA STRENGTH 1000

72 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:

GSK Consumer Healthcare

Warren, NJ 07059

105430XA (Front Label)

105431XA (Back Label)

INGREDIENTS AND APPEARANCE

TUMS ULTRA

calcium carbonate tablet, chewable

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:0135-0610
Route of Administration	ORAL

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

Ingredient Name	Strength
Inactive Ingredients
POWDERED CELLULOSE (UNII: SMD1X3XO9M)
DEXTROSE, UNSPECIFIED FORM (UNII: IY9XDZ35W2)
FD&C RED NO. 40 (UNII: WZB9127XOA)
ALUMINUM OXIDE (UNII: LMI26O6933)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
FD&C YELLOW NO. 6 (UNII: H77VEI93A8)
MALTODEXTRIN (UNII: 7CVR7L4A2D)
MINERAL OIL (UNII: T5L8T28FGP)
POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)
TALC (UNII: 7SEV7J4R1U)

Product Characteristics
Color	RED (red, yellow, orange, off white)	Score	no score
Shape	ROUND	Size	19mm
Flavor	TROPICAL FRUIT PUNCH (tropical fruit: tropical punch, banana, tropical orange, pineapple)	Imprint Code	TUMS
Contains

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:0135-0610-01	72 in 1 BOTTLE; Type 0: Not a Combination Product	09/01/2016
2	NDC:0135-0610-02	160 in 1 BOTTLE; Type 0: Not a Combination Product	09/01/2016

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph final	part331	09/01/2016

TUMS ULTRA

calcium carbonate tablet, chewable

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:0135-0612
Route of Administration	ORAL

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

Ingredient Name	Strength
Inactive Ingredients
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
Color	WHITE	Score	no score
Shape	ROUND	Size	19mm
Flavor	PEPPERMINT	Imprint Code	TUMS
Contains

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:0135-0612-01	72 in 1 BOTTLE; Type 0: Not a Combination Product	09/01/2016
2	NDC:0135-0612-02	160 in 1 BOTTLE; Type 0: Not a Combination Product	09/01/2016

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph final	part331	09/01/2016

Labeler - GlaxoSmithKline Consumer Healthcare Holdings (US) LLC (079944263)

Revised: 12/2020

Document Id: 23419246-72a9-4295-805d-4eb4eeab0327

Set id: ee3faeab-4cea-4852-9ddf-901a346c092a

Version: 4

Effective Time: 20201209

Search by Drug Name or NDC

NDC 00135-0610-02 TUMS 1000 mg/1 Details

TUMS 1000 mg/1

MedlinePlus Drug Summary

Product Information

Package

Package Images

NDC 00135-0610-02 (00135061002)

Contents

Standard Product Labeling (SPL)/Prescribing Information SPL ee3faeab-4cea-4852-9ddf-901a346c092a Details

Active ingredient (per tablet)

Purpose

Uses

Warnings

Ask a doctor or pharmacist before use if you are

When using this product

Keep out of reach of children.

Directions

Other information

Inactive ingredients (Tropical Fruit)

Inactive ingredient (Mint)

Questions?

Principal Display Panel

Principal Display Panel

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