SUNMARK Calcium Antacid description, usages, side effects, indications, overdosage, supplying and lots more!

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SUNMARK Calcium Antacid

McKesson

Sugar free calcium antacid Extra strength


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Active ingredient (in each tablet)

Calcium carbonate 750 mg

Purpose

Antacid

SUNMARK Calcium Antacid Uses

relieves:

  • acid indigestion
  • heartburn

Warnings

Ask a doctor or pharmacist before use if you are

  • presently taking a prescription drug. Antacids may interact with certain prescription drugs.

When using this product

do not take more than 10 tablets in a 24-hour period, or use the maximum dosage of this product for more than 2 weeks, except under the advice and supervision of a doctor.

keep out of reach of children.

Directions

  • chew 2-4 tablets as symptoms occur, or as directed by a doctor

SUNMARK Calcium Antacid Other information

  • store at room temperature. Phenylketonurics: contains phenylalanine, less than 1 mg per tablet

Inactive ingredients

adipic acid, aspartame, FD&C yellow 6 aluminum lake, flavor, magnesium stearate, maltodextrin, sorbitol

PDP

Compare to Tums E-X Sugar free active ingredient

sugar free

calcium antacid

Extra strength

calcium carbonate

calcium supplement

Fast relief of heartburn & acid indigestion

Natural and Artificial Flavor

Daily source of calcium

Orange Creme Flavor

80 Chewable TabletsSUNMARK Calcium Antacid

SUNMARK Calcium Antacid

SUNMARK Calcium Antacid

Calcium carbonate TABLET, CHEWABLE

Product Information

Product Type Human otc drug label Item Code (Source) NDC:49348-055
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
Adipic Acid
ASPARTAME
FD&C YELLOW NO. 6
MAGNESIUM STEARATE
maltodextrin
cellulose, microcrystalline
sorbitol

Product Characteristics

Color Size Imprint Code Shape
orange 16 mm G174 ROUND

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:49348-055-39 80 in 1 BOTTLE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part331 2013-08-08


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