CALCIUM CARBONATE tablet, chewable

Drug Labeling and Warnings

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Drug Facts

Active ingredient (In Each Tablet)

Calcium Carbonate USP 500mg

Purpose

Antacid

Use

temporarily relieves:

• ▪ Heartburn
• ▪ Sour Stomach
• ▪ Acid Indigestion
• ▪ Upset Stomach Associated With These Symptoms

Warnings

Ask a doctor before use if you have

• ▪ kidney disease
• ▪ taking any prescription drugs; antacids may interact with certain prescription drugs

When using this product do not take more than 15 tablets in a 24 hour period or use the maximum dosage of this product for more than 2 weeks.

If pregnant or breast-feeding, ask a health professional before use.

Keep out of reach of children.

Directions

Chew 2-4 tablets as symptoms occur, repeat hourly if needed

Other Information

• ▪ do not use if packet is opened or torn
• ▪ Store at controlled room temperature 15° to 30° C (59° to 86° F)
• ▪ Calcium content per tablet: 200mg

Inactive Ingredients

FD&C yellow #6 aluminum lake, magnesium stearate, maltodextrin, orange flavor, sorbitol

Questions?

1-866-651-3660 Monday-Friday 8:00am-5:00pm EST

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Overbagged with 10 chewable tablets per bag, NDC: 55154-6751-0

WARNING: This Unit Dose package is not child resistant and is Intended for Institutional Use Only. Keep this and all drugs out of the reach of children.

Mfg. by: Allegiant Health, Deer Park, NY 11729

Dist. By: Hospak® Unit Dose Products, Huntley, IL

60142

Hospak®

Distributed By:

Cardinal Health

Dublin, OH 43017

L33753910124

Principal Display Panel

NDC: 55154-6751-0

CALCIUM CARBONATE 500mg

(Calcium, Elemental 200mg)

CHEWABLE ANTACID TABLETS

10 TABLETS

INGREDIENTS AND APPEARANCE

CALCIUM CARBONATE 
calcium carbonate tablet, chewable

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 55154-6751
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CALCIUM CARBONATE (UNII: H0G9379FGK) (CALCIUM CATION - UNII:2M83C4R6ZB)	CALCIUM CARBONATE	500 mg

Inactive Ingredients
Ingredient Name	Strength
FD&C YELLOW NO. 6 ALUMINUM LAKE (UNII: GYP6Z2JR6Q)
MAGNESIUM STEARATE (UNII: 70097M6I30)
MALTODEXTRIN (UNII: 7CVR7L4A2D)
SORBITOL (UNII: 506T60A25R)

Product Characteristics
Color	ORANGE	Score	no score
Shape	ROUND	Size	15mm
Flavor	CITRUS	Imprint Code	RH;024
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 55154-6751-0	10 in 1 BAG	03/07/2018	10/31/2026
1		1 in 1 BLISTER PACK; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M001	03/07/2018	10/31/2026

Labeler - Cardinal Health 107, LLC (118546603)