CALCIUM CARBONATE CHEWABLE ANTACID- calcium carbonate tablet, chewable

CALCIUM CARBONATE CHEWABLE ANTACID by

Drug Labeling and Warnings

CALCIUM CARBONATE CHEWABLE ANTACID by is a Otc medication manufactured, distributed, or labeled by NuCare Pharmaceuticals,Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient (in each tablet)

Calcium Carbonate 500 mg

Purpose

Antacid

Uses

• temporarily relieves: acid indigestion, heartburn, sour stomach

Warnings

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.

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

Directions

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

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

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

INGREDIENTS AND APPEARANCE

CALCIUM CARBONATE CHEWABLE ANTACID 
calcium carbonate tablet, chewable

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 68071-4588(NDC:57896-763)
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	500 mg

Inactive Ingredients
Ingredient Name	Strength
DEXTROSE (UNII: IY9XDZ35W2)
MALTODEXTRIN (UNII: 7CVR7L4A2D)
D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)
FD&C YELLOW NO. 6 (UNII: H77VEI93A8)
FD&C RED NO. 40 (UNII: WZB9127XOA)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
MAGNESIUM STEARATE (UNII: 70097M6I30)

Product Characteristics
Color	red, green, orange, yellow	Score	no score
Shape	ROUND	Size	14mm
Flavor	CHERRY, LIME, ORANGE, LEMON	Imprint Code	AZ;024
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 68071-4588-5	150 in 1 BOTTLE; Type 0: Not a Combination Product	10/05/2018

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part331	01/01/2004

Labeler - NuCare Pharmaceuticals,Inc. (010632300)

Establishment
Name	Address	ID/FEI	Business Operations
NuCare Pharmaceuticals,Inc.		010632300	relabel(68071-4588)