Antacid Antigas Maximum Strength Original description, usages, side effects, indications, overdosage, supplying and lots more!

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Antacid Antigas Maximum Strength Original

Aaron Industries, Inc.
Aaron Industries, Inc.

Drug Facts


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Active ingredients

Aluminum hydroxide(equivalent to Dried Gel, USP) 400 mg
Magnesium hydroxide 400 mg
Simethicone 40 mg

Purpose

Antacid
Antigas

Antacid Antigas Maximum Strength Original Uses

relieves: • heartburn • sour stomach • acid indigestion
• upset stomach due to these symptoms • symptoms of 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

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

Stop use and ask a doctor

if symptoms last for more
than 2 weeks

If pregnant or breast-feeding

ask a health professional before use.

Keep this and all drugs out of the reach of children.

In case of accidental overdose, seek professional assistance
or contact a Poison Control Center immediately.

Directions

shake well before use
• do not exceed 12 teaspoons (60 mL) in a 24 hour period or
use the maximum dosage for more than 2 weeks
• adults and children 12 years of age and older: take 2 to 4
teaspoons (10-20 mL) between meals and at
bed time or as directed by a doctor
• children under 12 years of age: ask a doctor

Other Information

do not freeze
• store at room temperature tightly closed
• each teaspoon contains:
potassium 2 mg, magnesium 167 mg

Inactive Ingredients

benzyl alcohol,
flavors, glycerin, hydroxyethyl cellulose,
potassium citrate, propylene glycol,
purified water, sorbitol

Principal Display Panel

This product is not manufactured or distributed by Johnson and Johnson merck, distributor of Mylanta



Antacid Antigas Maximum Strength Original

Antacid Antigas Maximum Strength Original

Antacid Antigas Maximum Strength Mylanta Original SUSPENSION

Product Information

Product Type Human otc drug label Item Code (Source) NDC:49580-0122
Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
aluminum hydroxide 400 mg
magnesium hydroxide MAGNESIUM CATION 400 mg
DIMETHICONE 40 mg

Inactive Ingredients

Ingredient Name Strength
GLYCERIN
HYDROXYETHYL CELLULOSE (2000 CPS AT 1%)
POTASSIUM CITRATE
propylene glycol
sorbitol

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:49580-0122-2 355 in 1 BOTTLE, PLASTIC

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part331 2009-04-09


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