Search by Drug Name or NDC

NDC 00135-0184-01 Tums Chewy Bites 750 mg/1 Details

Tums Chewy Bites 750 mg/1

Tums Chewy Bites 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: 00135-0184-01
Last Updated: 11/30/2022
MedLinePlus Full Drug Details: Calcium Carbonate

Product Information

NDC	00135-0184
Product ID	0135-0184_9043983c-7ee4-4971-8885-36f814bb570f
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 Chewy Bites
Proprietary Name Suffix	Berry Shake
Non-Proprietary Name	calcium carbonate
Product Type	HUMAN OTC DRUG
Dosage Form	TABLET, CHEWABLE
Route	ORAL
Active Ingredient Strength	750
Active Ingredient Units	mg/1
Substance Name	CALCIUM CARBONATE
Labeler Name	GlaxoSmithKline Consumer Healthcare Holdings (US) LLC
Pharmaceutical Class	Blood Coagulation Factor [EPC], Calcium [CS], Cations, Divalent [CS], Increased Coagulation Factor Activity [PE]
DEA Schedule	n/a
Marketing Category	OTC MONOGRAPH FINAL
Application Number	part331
Listing Certified Through	2024-12-31

Package

Package Images

NDC 00135-0184-01 (00135018401)

Pricing Information	N/A
NDC Package Code	0135-0184-01
Billing NDC	00135018401
Package	1 BOTTLE in 1 CARTON (0135-0184-01) / 32 TABLET, CHEWABLE in 1 BOTTLE
Marketing Start Date	2021-07-01
NDC Exclude Flag	N

Standard Product Labeling (SPL)/Prescribing Information SPL 9043983c-7ee4-4971-8885-36f814bb570f Details

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 6 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 chewable tablet contains: elemental calcium 305 mg
•: do not store above 25°C (77°F)

Inactive ingredients

Acacia gum, alcohol, ammonium hydroxide, beeswax, carmine, carnauba wax, citric acid, coconut oil, corn starch, corn syrup, dextrin, ethyl acetate, ethyl alcohol, FD&C blue no. 1 aluminum lake, FD&C blue no. 2 aluminum lake, FD&C red no. 40 aluminum lake, FD&C yellow no. 6 aluminum lake, flavors, gum arabic, isopropyl alcohol, maltodextrin, methyl paraben, n-butyl alcohol, phosphoric acid, propylene glycol, propylparaben, purified water, shellac, sorbic acid, sorbitol, soybean oil, soy lecithin, sucrose, tertiary butylhydroquinone, titanium dioxide, vegetable oil

Questions or comments?

Call 1-800-897-7535

Principal Display Panel

NDC 0135-0184-01

TUMS

CALCIUM CARBONATE

ANTACID

Chewy Bites

Berry Shake

GOES TO WORK IN SECONDS!

EXTRA STRENGTH 750

32 CHEWABLE TABLETS

Safety sealed –

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

Distributed by:

GSK Consumer Healthcare

Warren, NJ 07059

Trademarks are owned by or licensed to the GSK group of companies.

Front Label: 1001083

Back Label: 1001084

INGREDIENTS AND APPEARANCE

TUMS CHEWY BITES BERRY SHAKE

calcium carbonate tablet, chewable

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:0135-0184
Route of Administration	ORAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
CALCIUM CARBONATE (UNII: H0G9379FGK) (CALCIUM CATION - UNII:2M83C4R6ZB, CARBONATE ION - UNII:7UJQ5OPE7D)	CALCIUM CARBONATE	750 mg

Ingredient Name	Strength
Inactive Ingredients
ACACIA (UNII: 5C5403N26O)
ALCOHOL (UNII: 3K9958V90M)
AMMONIA (UNII: 5138Q19F1X)
YELLOW WAX (UNII: 2ZA36H0S2V)
CARMINIC ACID (UNII: CID8Z8N95N)
CARNAUBA WAX (UNII: R12CBM0EIZ)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
COCONUT OIL (UNII: Q9L0O73W7L)
STARCH, CORN (UNII: O8232NY3SJ)
CORN SYRUP (UNII: 9G5L16BK6N)
ICODEXTRIN (UNII: 2NX48Z0A9G)
ETHYL ACETATE (UNII: 76845O8NMZ)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
ALUMINUM OXIDE (UNII: LMI26O6933)
FD&C BLUE NO. 2 (UNII: L06K8R7DQK)
FD&C RED NO. 40 (UNII: WZB9127XOA)
FD&C YELLOW NO. 6 (UNII: H77VEI93A8)
ISOPROPYL ALCOHOL (UNII: ND2M416302)
MALTODEXTRIN (UNII: 7CVR7L4A2D)
METHYLPARABEN (UNII: A2I8C7HI9T)
BUTYL ALCOHOL (UNII: 8PJ61P6TS3)
PHOSPHORIC ACID (UNII: E4GA8884NN)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
PROPYLPARABEN (UNII: Z8IX2SC1OH)
WATER (UNII: 059QF0KO0R)
SHELLAC (UNII: 46N107B71O)
SORBIC ACID (UNII: X045WJ989B)
SORBITOL (UNII: 506T60A25R)
SOYBEAN OIL (UNII: 241ATL177A)
LECITHIN, SOYBEAN (UNII: 1DI56QDM62)
SUCROSE (UNII: C151H8M554)
TERT-BUTYLHYDROQUINONE (UNII: C12674942B)
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
CORN OIL (UNII: 8470G57WFM)

Product Characteristics
Color	PINK	Score	no score
Shape	ROUND	Size	19mm
Flavor	BERRY (Shake)	Imprint Code	T
Contains

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:0135-0184-01	1 in 1 CARTON	07/01/2021
1		32 in 1 BOTTLE; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph final	part331	03/05/2021

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

Revised: 6/2021

Document Id: 9043983c-7ee4-4971-8885-36f814bb570f

Set id: 9043983c-7ee4-4971-8885-36f814bb570f

Version: 1

Effective Time: 20210609