GERI-LANTA MAXIMUM STRENGTH description, usages, side effects, indications, overdosage, supplying and lots more!

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GERI-LANTA MAXIMUM STRENGTH

Geri-Care Pharmaceuticals, Corp
GCP Laboratories


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Active ingredients (in each 5 mL teaspoonful)




Purposes

Antacid

Antigas

GERI-LANTA MAXIMUM STRENGTH Uses


  • heartburn
  • sour stomach
  • acid indigestion
  • the symptoms referred to as gas

Warnings

Ask a doctor before use if you have



Ask a doctor or pharmacist before use if you are



Stop use and ask a doctor if

If pregnant or breast-feeding,

Keep out of reach of children.

Directions





GERI-LANTA MAXIMUM STRENGTH Other information

each 5 mL teaspoonful contains: magnesium 165 mg, sodium 1 mg
• store at room temperature

• protect from freezing
 • keep tightly closed

TAMPER-EVIDENT: Do not use if breakaway band on bottle is missing or broken.

Inactive ingredients

benzyl alcohol, butylparaben, carboxymethylcellulose sodium, flavor (contains alcohol), hypromellose, microcrystalline cellulose, propylparaben, purified water, saccharin sodium, sorbitol solution

package Label

NDC 57896-619-12

GERICARE

Maximum Strength

GERI-LANTA

antacid/antigas

Alumina, Magnesia and Simethicone Oral Suspension

For Relief of:

HEARTBURN

SOUR STOMACH

ACID INDIGESTION

GAS

compare to the active ingredients in Maximum Strength MYLANTA

12 FL OZ (355 mL)

Alcohol: 0.5%

GERI-LANTA MAXIMUM STRENGTH

GERI-LANTA MAXIMUM STRENGTH

aluminum hydroxide, magnesium hydroxide, dimethicone LIQUID

Product Information

Product Type Human otc drug label Item Code (Source) NDC:57896-619
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
BENZYL ALCOHOL
BUTYLPARABEN
CARBOXYMETHYLCELLULOSE SODIUM
HYPROMELLOSES
cellulose, microcrystalline
PROPYLPARABEN
water
SACCHARIN SODIUM DIHYDRATE
sorbitol

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:57896-619-12 355 in 1 BOTTLE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part331 2000-01-01


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