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

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sunmark antacid

McKesson

McKesson Antacid Drug Facts


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Active ingredient (in each 5 mL teaspoon)

Aluminum hydroxide (equiv. to dried gel, USP) 400 mg

Magnesium hydroxide 400 mg

Simethicone 40 mg

Purpose

Antacid

Antigas

sunmark antacid 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

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

When using this product

do not exceed 12 teaspoonsful (60 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 before use
  • adults and children 12 years and older: take 2-4 teaspoonsful (10-20 mL) between meals, at bedtime, or as directed by a doctor
  • children under 12: ask a doctor

sunmark antacid Other information

  • each teaspoon contains: calcium 50 mg, magnesium 175 mg, potassium 10 mg and sodium 2 mg
  • does not meet USP requirements for preservative effectiveness
  • store at 20°-25°C

Inactive ingredients

butylparaben, carboxymethylcellulose sodium, flavor, hypromellose, microcrystalline cellulose, potassium citrate, propylparaben, purified water, simethicone emulsion, sorbitol

Principal Display Panel

Compare to Mylanta® Maximum Strength Active Ingredients

Antacid

Maximum Strength

Antacid/Anti-Gas

Fast Acting

Fast soothing relief of heartburn, acid indigestion, sour stomach & gas

Original

sunmark antacid
Antacid Front Label Antacid Back Label

sunmark antacid

aluminum hydroxide, magnesium hydroxide, simethicone LIQUID

Product Information

Product Type Human otc drug label Item Code (Source) NDC:49348-035
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
SILICON DIOXIDE
BUTYLPARABEN
CARBOXYMETHYLCELLULOSE SODIUM
HYPROMELLOSES
cellulose, microcrystalline
POTASSIUM CITRATE
PROPYLPARABEN
water
sorbitol

Product Characteristics

Color
WHITE (opaque)

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:49348-035-39 355 in 1 BOTTLE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part331 2003-10-20


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