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Tums

GlaxoSmithKline Consumer Heathcare LP

Drug Facts


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Calcium carbonate USP 750 mg

Antacid

relieves

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

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

Keep out of reach of children.

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

  • •for calcium/magnesium/sodium content see Supplement Facts
  • •store below 25oC (77oF). Keep the container tightly closed.

calcium carbonate, sorbitol, dextrose, sucrose, microcrystalline cellulose, magnesium stearate, natural and artificial flavors, adipic acid, corn starch, guar gum, maltodextrin, red 40 lake, blue 1 lake. Contains soy

1-800-897-7535 weekdays

CALCIUM SUPPLEMENT

USES: As a daily source of extra calcium.

DIRECTIONS: Chew 2 tablets twice daily with a meal.

Supplement Facts

Serving Size: 2 Tablets

Servings Per Container: 30

Amount Per Serving

%Daily Value

Calories 10

Sugars 2g

Calcium 600mg

60%

Sodium 5mg

(less than 1%)

Magnesium 2mg

(less than 1%)

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

Gluten-Free

GlaxoSmithKline

Consumer Healthcare, L.P.

Moon Township, PA 15108

TUMS and SMOOTHIES are trademarks of the GlaxoSmithKline group of companies.

www.tums.com

Principal Display Panel

NDC 0135-0555-01

TUMS®

EXTRA STRENGTH 750

ANTACID

ASSORTED FRUIT

8 Chewable TABLETS

TUMS®

ANTACID / CALCIUM SUPPLEMENT

Smoothies TM

EXTRA STRENGTH 750

CALCIUM RICH

SMOOTH DISSOLVE

BERRY FUSION

NATURALLY & ARTIFICIALLY FLAVORED

PAREVE

FREE TUMS®

8ct Roll

60ct Bottle – Smoothies Berry Fusion

8ct Roll – EX Assorted Fruit

©2012 GlaxoSmithKline

102777PA

Tums

calcium carbonate KIT

Product Information

Product Type Human otc drug label Item Code (Source) NDC:0135-0555
Route of Administration DEA Schedule

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:0135-0555-01 1 in 1 CARTON

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part331 2013-04-12


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Be sure to consult your doctor before taking any medication!
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