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

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rexall antacid

Dolgencorp, LLC

Dolgencorp, LLC Antacid Chews Drug Facts


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Active ingredient (in each tablet)

Calcium carbonate USP 750mg

Purpose

Antacid

rexall antacid Uses

relieves

  • heartburn
  • sour stomach
  • acid indigestion
  • upset stomach associated with these symptoms

Warnings

Ask a doctor before use if you have

  • kidney stones
  • a calcium-restricted diet

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 take more than 10 tablets in 24 hours
  • do not use the maximum dosage for more than 2 weeks

Keep out of reach of children.

Directions

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

rexall antacid Other information

  • each tablet contains: calcium 320 mg and magnesium 10 mg
  • store at 20 - 25°C (68 - 77°F)

Inactive ingredients

blue #1 aluminum lake, dextrose, flavors, maltodextrin, mineral oil, polyethylene glycol, powdered cellulose, red #40 aluminum lake, talc

Principal Display Panel

EXTRA STRENGTH

Antacid Chews

Calcium Carbonate

Antacid/Calcium Supplement

DO NOT USE IF PRINTED SEAL UNDER CAP IS BROKEN OR MISSING

Assorted Berries

Naturally and Artificially Flavored

750 mg

rexall antacid
Antacid Chews Front Label Antacid Chews Back Label

rexall antacid

Calcium carbonate TABLET, CHEWABLE

Product Information

Product Type Human otc drug label Item Code (Source) NDC:55910-708
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
Mineral Oil
POLYETHYLENE GLYCOLS
POWDERED CELLULOSE
talc

Product Characteristics

Color Size Imprint Code Shape
PURPLE (violet) 17 mm L489 ROUND

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:55910-708-82 200 in 1 BOTTLE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part331 2011-05-10


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Be sure to consult your doctor before taking any medication!
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