CALCIUM CARBONATE CHEWABLE ANTACID description, usages, side effects, indications, overdosage, supplying and lots more!

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CALCIUM CARBONATE CHEWABLE ANTACID

Geri-Care Pharmaceutical Corp
Geri-Care Pharmaceutical Corp


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Active ingredient (in each tablet)

Calcium Carbonate 500 mg

Purpose

Antacid

CALCIUM CARBONATE CHEWABLE 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

CALCIUM CARBONATE CHEWABLE ANTACID 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



CALCIUM CARBONATE
CHEWABLE ANTACID




CALCIUM CARBONATE CHEWABLE ANTACID

CALCIUM CARBONATE CHEWABLE ANTACID

calcium carbonate TABLET, CHEWABLE

Product Information

Product Type Human otc drug label Item Code (Source) NDC:57896-763
Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
CALCIUM CARBONATE 500 mg

Inactive Ingredients

Ingredient Name Strength
DEXTROSE
maltodextrin
D&C YELLOW NO. 10
FD&C YELLOW NO. 6
FD&C RED NO. 40
FD&C BLUE NO. 1
MAGNESIUM STEARATE

Product Characteristics

Color Size Imprint Code Shape
yellow 14 mm AZ;024 ROUND

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:57896-763-15 150 in 1 BOTTLE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part331 2004-01-01


PLEASE, BE CAREFUL!
Be sure to consult your doctor before taking any medication!
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