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

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Antacid

H E B

HEB Antacid Drug Facts


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Active ingredient (in each tablet)

Calcium carbonate 1000 mg

Purpose

Antacid

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

Antacid 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 Maximum Strength Tums Ultra® Assorted Fruit Flavors active ingredient

ANTACID

Ultra Strength - 1000

Calcium Carbonate 1000 mg

Antacid/Calcium Supplement

Assorted Fruit

Naturally and artificially flavored

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

Antacid
Antacid Front Label Antacid Back Label

Antacid

Calcium Carbonate TABLET, CHEWABLE

Product Information

Product Type Human otc drug label Item Code (Source) NDC:37808-595
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
FD&C BLUE NO. 1
FD&C RED NO. 40
FD&C YELLOW NO. 5
FD&C YELLOW NO. 6
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:37808-595-23 72 in 1 BOTTLE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part331 1995-11-14


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Be sure to consult your doctor before taking any medication!
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