CALCIUM CARBONATE CHEWABLE ANTACID

Manufacturer: NuCare Pharmaceuticals,Inc.
Effective date: 2019-10-04
Label type: HUMAN OTC DRUG LABEL
Version: 3
Source: legacy-cache
Hydrated at: 2026-08-02 00:08:34

Label at a glance#

ProductCALCIUM CARBONATE CHEWABLE ANTACID

Active ingredientCALCIUM CARBONATE

Label structure8 sections

Indications and uses

temporarily relieves: acid indigestion, heartburn, sour stomach

Dosage and administration

• do not exceed recommended dose • adults and children 12 years of age and older: chew 2-4 tablets as symptoms occur • repeat hourly if symptoms return, or as directed by a physician • do not take more than 15 tablets in a 24 hour period • children under 12 years: consult a doctor

Storage and handling

• each tablet contains: calcium 200 mg • store at room temperature • for institutional use only • Tamper Evident: Do not use if imprinted seal under cap is missing or broken.

Label contents#

Full prescribing information#

Active ingredient (in each tablet)

OTC - ACTIVE INGREDIENT SECTION

Calcium Carbonate 500 mg

Purpose

OTC - PURPOSE SECTION

Antacid

Uses

INDICATIONS & USAGE SECTION

temporarily relieves: acid indigestion, heartburn, sour stomach

Warnings

WARNINGS SECTION

Ask a doctor before use if you
• have kidney disease
• are taking prescription drugs; antacids may interact with certain prescription drugs

Stop use and ask a doctor if • symptoms last more than 2 weeks.

When using this product • do not use the maximum dosage for more than 2 weeks

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

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

• do not exceed recommended dose
• adults and children 12 years of age and older: chew 2-4 tablets as symptoms occur
• repeat hourly if symptoms return, or as directed by a physician
• do not take more than 15 tablets in a 24 hour period
• children under 12 years: consult a doctor

Other information

STORAGE AND HANDLING SECTION

• each tablet contains: calcium 200 mg
• store at room temperature
• for institutional use only
• Tamper Evident: Do not use if imprinted seal under cap is missing or broken.

Inactive ingredients

INACTIVE INGREDIENT SECTION

assorted flavors, dextrose, D and C Yellow no. 10 lake, FD and C Blue no. 1 lake, FD and C Red no. 40 lake, FD and C Yellow no. 6 lake, magnesium stearate, maltodextrin. May also contain cellulose, FD and C Yellow no. 5 lake (tartrazine), stearic acid, sugar.

Package label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

pdp

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
68071-4588-5	2024-06-12	C162847	48780-1	ba0f9c33-335d-a910-e053-dadaa90a0b85	7782cdf0-361c-421d-e053-2a91aa0af366
68071-4588-5	2021-01-29	C162847	48780-1	ba0f9c33-335d-a910-e053-dadaa90a0b85	7782cdf0-361c-421d-e053-2a91aa0af366

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
57896-763-15	EA - Each	57896-763	bd024f8c-2db5-482e-81d6-da9a1d45ca7b	1	2013-12-02

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 11 matching rows.

CALCIUM CARBONATE CHEWABLE ANTACID
calcium carbonate
DEXTROSE
MALTODEXTRIN
D&C YELLOW NO. 10
FD&C YELLOW NO. 6
FD&C RED NO. 40
FD&C BLUE NO. 1
MAGNESIUM STEARATE
CALCIUM CATION
CARBONATE ION

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
68071-4588	68071-4588-5
57896-763

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
DEXTROSE	IY9XDZ35W2	IACT
MALTODEXTRIN	7CVR7L4A2D	IACT
D&C YELLOW NO. 10	35SW5USQ3G	IACT
FD&C YELLOW NO. 6	H77VEI93A8	IACT
FD&C RED NO. 40	WZB9127XOA	IACT
FD&C BLUE NO. 1	H3R47K3TBD	IACT
MAGNESIUM STEARATE	70097M6I30	IACT
CALCIUM CARBONATE	H0G9379FGK	ACTIB

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 2 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
1ab55b81-219b-1137-e063-6294a90af88a			7782cdf0-361c-421d-e053-2a91aa0af366	2024-06-12	Warnings	Exact identifier spl set id: 7782cdf0-361c-421d-e053-2a91aa0af366
CALCIUM CARBONATE CHEWABLE ANTACID	CALCIUM CARBONATE	Geri-Care Pharmaceutical Corp	27d9b505-08bd-4261-a59d-6ddc4031be32	2023-10-25	Warnings	Exact identifier ndc (product): 57896-763

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.