extra strength description, usages, side effects, indications, overdosage, supplying and lots more!

extra strength

Publix Super Markets Inc

  • 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
Publix Super Markets, Inc. Extra Strength Drug Facts

FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Active ingredient (in each tablet)

Calcium carbonate USP 750mg

Purpose

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

Other information

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

Inactive ingredients

dextrose, flavors, maltodextrin, mineral oil, polyethylene glycol, powdered cellulose, red #40 aluminum lake, talc, yellow #5 aluminum lake (tartrazine), yellow #6 aluminum lake

Principal Display Panel

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

extra strength

ANTACID CALCIUM SUPPLEMENT

CALCIUM CARBONATE 750mg

ASSORTED TROPICAL FRUIT

NATURALLY & ARTIFICIALLY FLAVORED

Compare to Active Ingredient in Tums® Extra Strength 750 Assorted Tropical Fruit Flavors

Principal Display Panel
Extra Strength Front Label Extra Strength Back Label

extra strength

Calcium carbonate TABLET, CHEWABLE

Product Information

Product Type Human otc drug label Item Code (Source) NDC:56062-468
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
RED 17 mm L468 ROUND

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:56062-468-80 96 in 1 BOTTLE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part331 2002-05-09


PLEASE, BE CAREFUL!
Be sure to consult your doctor before taking any medication!
Copyright © 2014. drugs-library.com. All rights reserved. Information on drugs-library.com is provided for educational purposes only and is not to be used for medical advice, diagnosis or treatment.
Support info@drugs-library.com.