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

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ANTACID

Target Corporation

Drug Facts


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Calcium carbonate USP 1,000 mg

Antacid

relieves

  • •heartburn
  • •acid indigestion

Ask a doctor or pharmacist before use if you are

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

When using this product

  • •do not take more than 7 tablets in 24 hours
  • •do not use the maximum dosage for more than 2 weeks

Keep out of reach of children.

  • •chew 2-3 tablets as symptoms occur, or as directed by a doctor
  • •for calcium and sodium content see Supplement Facts
  • •store below 30oC (86oF)
  • •(Assorted Fruit) each tablet provides 400mg of elemental calcium

sucrose, calcium carbonate, corn starch, talc, mineral oil, natural and artificial flavors, adipic acid, sodium polyphosphate, red 40 lake, yellow 6 lake, yellow 5 (tartrazine) lake, blue 1 lake

sucrose, calcium carbonate, corn starch, talc, mineral oil, natural flavor, sodium polyphosphate

Call 1-888-367-7919

Principal Display Panel

NDC 11673-481-83

antacid tablets

ultra strength

antacid/calcium supplement

Compare to active ingredients in Tums Ultra®* 

up&upTM

assorted fruit flavor

72 CHEWABLE TABLETS

naturally and artificially flavored

CALCIUM SUPPLEMENT

USES: As a daily source of extra calcium.

DIRECTIONS: Chew 2 tablets once or twice daily with a meal.

Supplement Facts

Serving Size: 2 Tablets

Servings Per Container: 36

Amount Per Serving

% Daily Value

Calories 10

Sugars 3g

Calcium 800mg

80%

Sodium 10mg

Less than 1%

Safety sealed- Do not use if printed inner seal beneath cap is missing or broken.

*TUMS and TUMS ULTRA are registered trademarks of the GlaxoSmithKline group of companies.

245 05 0454 ID271409

Distributed by Target Corporation

Minneapolis, MN 55403

©2011 Target Brands, Inc.

All Rights Reserved

Shop Target.com

Gluten-Free

71731XD (front label)

66700XC (back label)

Principal Display Panel

NDC 11673-722-01

antacid tablets

ultra strength antacid/calcium supplement

calcium carbonate, 1,000 mg

Compare to active ingredient in TUMS® Ultra*

up & up®

160 CHEWABLE TABLETS

naturally flavored

peppermint flavor

CALCIUM SUPPLEMENT

USES: As a daily source of extra calcium.

DIRECTIONS: Chew 2 tablets once or twice daily with a meal.

Supplement Facts

Serving Size: 2 Tablets

Servings Per Container: 80

Amount Per Serving

%Daily Value

Calories 10

Sugars 3g

Calcium 800mg

80%

Sodium 10mg

Less than 1%

Safety sealed- Do not use if printed inner seal beneath cap is missing or broken.

*TUMS and TUMS ULTRA are registered trademarks of the GlaxoSmithKline group of companies.

245 05 0049 ID083403

Dist. by Target Corporation

Minneapolis, MN 55403

©2013 Target Brands, Inc.

Shop Target.com

Guest Services 1-800-910-6874

GLUTEN FREE

Front Label: 102801XA

Back Label: 102802XA

ANTACID

calcium carbonate TABLET

Product Information

Product Type Human otc drug label Item Code (Source) NDC:11673-481
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
SUCROSE
STARCH, CORN
talc
Mineral Oil
Adipic Acid
SODIUM POLYMETAPHOSPHATE
FD&C RED NO. 40
FD&C YELLOW NO. 6
FD&C YELLOW NO. 5
FD&C BLUE NO. 1
ALUMINUM OXIDE

Product Characteristics

Color Size Imprint Code Shape
PINK (orange, yellow, green) 19 mm LH20 ROUND

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:11673-481-83 72 in 1 BOTTLE
2 NDC:11673-481-14 160 in 1 BOTTLE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part331 2010-02-15


ANTACID

calcium carbonate TABLET

Product Information

Product Type Human otc drug label Item Code (Source) NDC:11673-722
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
SUCROSE
STARCH, CORN
talc
Mineral Oil
SODIUM POLYMETAPHOSPHATE

Product Characteristics

Color Size Imprint Code Shape
WHITE 19 mm LH20 ROUND

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:11673-722-01 160 in 1 BOTTLE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part331 2013-03-08


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