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

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CALCIUM CARBONATE EXTRA STRENGTH ANTACID

Geri-Care Pharmaceutical Corp
Geri-Care Pharmaceutical Corp


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Active ingredient (in each tablet)

Calcium Carbonate 750 mg

Purpose

Antacid

CALCIUM CARBONATE EXTRA STRENGTH 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 take more than 10 tablets in 24 hours

• 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 10 tablets in a 24 hour period

• children under 12 years: consult a doctor

CALCIUM CARBONATE EXTRA STRENGTH ANTACID Other information

each tablet contains: calcium 300 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.

Package label

GERICARE

NDC 57896-764-96

CALCIUM CARBONATE

EXTRA STRENGTH
CHEWABLE ANTACID

ASSORTED FLAVORS

compare to active ingredient in TUMS extra strength tablets

96 Tablets

750 mg each


CALCIUM CARBONATE EXTRA STRENGTH ANTACID

CALCIUM CARBONATE EXTRA STRENGTH ANTACID

calcium carbonate TABLET, CHEWABLE

Product Information

Product Type Human otc drug label Item Code (Source) NDC:57896-764
Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
CALCIUM CARBONATE 750 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 15 mm RH031 ROUND

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:57896-764-96 96 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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