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

Sunmark Calcium Antacid

McKesson

  • Description
  • Clinical Pharmacology
  • Indications & Usage
  • Contraindications
  • Warnings
  • Precautions
  • Side Effects
  • Overdosage
  • Dosage & Administration
  • How Supplied
  • Patient Counseling Information
  • Supplemental Patient Material
  • Boxed Warning
  • Patient Package Insert
McKesson Calcium Antacid Drug Facts

FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Active ingredient (in each tablet)

Calcium carbonate 1000 mg

Purpose

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 7 tablets daily or use the maximum dosage for more than 2 weeks

Keep out of reach of children.

Directions

chew 2 to 3 tablets as symptoms occur

Other information

  • each tablet contains: calcium 425 mg and magnesium 10 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 ULTRA® ACTIVE INGREDIENT

calcium antacid

Ultra Strength

Chewable

Antacid & Calcium Supplement

1000 mg Calcium Carbonate

Naturally & artificially flavored

ASSORTED FRUIT FLAVORS

Principal Display Panel
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:49348-195
Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
CALCIUM CARBONATE 1000 mg

Inactive Ingredients

Ingredient Name Strength
Adipic Acid
DEXTROSE
maltodextrin
Mineral Oil
POLYETHYLENE GLYCOLS
POWDERED CELLULOSE
talc

Product Characteristics

Color Size Imprint Code Shape
ORANGE 20 mm L595 ROUND

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:49348-195-16 72 in 1 BOTTLE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part331 2003-07-15


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Be sure to consult your doctor before taking any medication!
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