Sunmark calcium antacid description, usages, side effects, indications, overdosage, supplying and lots more!

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Sunmark calcium antacid

McKesson

McKesson Calcium Antacid Drug Facts


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Active ingredient (in each tablet)

Calcium carbonate 500 mg

Purpose

Antacid

Sunmark calcium antacid Uses

relieves

  • heartburn
  • sour stomach
  • acid indigestion

Warnings

Ask a doctor or pharmacist before use if you are

now taking a prescription drug. Antacids may interact with certain prescription drugs.

When using this product

do not exceed 15 tablets daily or use the maximum dosage for more than 2 weeks

Keep out of reach of children.

Directions

chew 2 to 4 tablets as symptoms occur

Other information

  • each tablet contains: calcium 215 mg and magnesium 5 mg
  • store at 20°-25°C (68°-77°F)

Inactive ingredients

adipic acid, dextrose, FD&C blue #1 aluminum lake, FD&C red #40 aluminum lake, FD&C yellow #5 aluminum lake (tartrazine), FD&C yellow #6 aluminum lake, flavors, maltodextrin, mineral oil, polyethylene glycol, powdered cellulose, talc

Questions?

1-800-719-9260

Principal Display Panel

COMPARE TO TUMS® ACTIVE INGREDIENT

calcium antacid

Regular Strength

Chewable

Antacid & Calcium Supplement

500 mg Calcium Carbonate

Naturally & artificially flavored

ASSORTED FRUIT FLAVORS

Sunmark calcium antacid
Calcium Antacid Front Label Calcium Antacid Back Label

Sunmark calcium antacid

calcium carbonate TABLET, CHEWABLE

Product Information

Product Type Human otc drug label Item Code (Source) NDC:49348-170
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
Adipic Acid
DEXTROSE
FD&C BLUE NO. 1
FD&C RED NO. 40
FD&C YELLOW NO. 5
FD&C YELLOW NO. 6
maltodextrin
Mineral Oil
POLYETHYLENE GLYCOLS
POWDERED CELLULOSE
talc

Product Characteristics

Color Size Imprint Code Shape
ORANGE 17 mm L478 ROUND

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:49348-170-21 150 in 1 BOTTLE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part331 2003-08-21


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Be sure to consult your doctor before taking any medication!
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