up and up antacid anti gas description, usages, side effects, indications, overdosage, supplying and lots more!

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up and up antacid anti gas

Target Corporation

Target Corporation Regular Strength Antacid Anti-Gas Drug Facts


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Active ingredients (in each 5 mL teaspoon)

Aluminum hydroxide (equiv. to dried gel, USP) 200 mg

Magnesium hydroxide 200 mg

Simethicone 20 mg

Purposes

Antacid

Antigas

up and up antacid anti gas Uses

relieves

  • •heartburn
  • •acid indigestion
  • •sour stomach
  • •upset stomach due to these symptoms
  • •pressure and bloating commonly referred to as gas

Warnings

Ask a doctor before use if you have

  • •kidney disease
  • •a magnesium-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 exceed 24 teaspoonfuls (120 mL) in a 24-hour period, or use the maximum dosage for more than 2 weeks, unless directed by a doctor

Keep out of reach of children.

Directions

  • •shake well
  • •adults and children 12 years and older: take 2-4 teaspoonfuls (10-20 mL) between meals, at bedtime, or as directed by a doctor
  • •children under 12 years: ask a doctor

up and up antacid anti gas Other information

  • •each teaspoon contains: magnesium 85 mg
  • •does not meet USP requirements for preservative effectiveness
  • •store at 20°-25°C (68°-77°F)

Inactive ingredients

butylparaben, flavor, hypromellose, microcrystalline cellulose and carboxymethylcellulose sodium, peppermint oil, propylparaben, purified water, simethicone emulsion, sorbitol, sorbitol solution

Questions?

Call 1-800-910-6874

Principal Display Panel

antacid anti-gas

regular strength

fast acting

Compare to active ingredients in Regular Strength Mylanta®

soothing relief of

heartburn

acid indigestion

sour stomach

classic original flavor

ALCOHOL 0.2%

12 FL OZ (355 ml)

up and up antacid anti gas

Aluminum hydroxide, Magnesium hydroxide, Simethicone LIQUID

Product Information

Product Type Human otc drug label Item Code (Source) NDC:11673-357
Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
aluminum hydroxide 200 mg
magnesium hydroxide MAGNESIUM CATION 200 mg
DIMETHICONE 20 mg

Inactive Ingredients

Ingredient Name Strength
SILICON DIOXIDE
BUTYLPARABEN
CARBOXYMETHYLCELLULOSE SODIUM
HYPROMELLOSES
cellulose, microcrystalline
PROPYLPARABEN
water
sorbitol
PEPPERMINT OIL

Product Characteristics

Color
WHITE (opaque)

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:11673-357-40 355 in 1 BOTTLE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part332 2009-06-16


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Be sure to consult your doctor before taking any medication!
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