GERI-LANTA SUPREME CHERRY description, usages, side effects, indications, overdosage, supplying and lots more!

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GERI-LANTA SUPREME CHERRY

Geri-Care Pharmaceuticals, Corp
GCP Laboratories


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Active ingredients (in each 5 mL teaspoonful)

Calcium carbonate 400 mg
Magnesium hydroxide 135 mg

Purpose

Antacid

GERI-LANTA SUPREME CHERRY Uses

relieves

  • heartburn
  • sour stomach
  • acid indigestion
  • upset stomach associated with these symptoms

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.

Stop use and ask a doctor if symptoms last more than 2 weeks

If pregnant or breast-feeding, ask a health professional before use.

Keep out of reach of children.

Directions

• shake well before use
• adults and children 12 years and older: take 2 to 4 teaspoonfuls between meals, at bedtime, or as directed by a doctor
• do not take more than 18 teaspoonfuls in 24 hours or use the maximum dosage for more than 2 weeks
• children under 12 years: ask a doctor

GERI-LANTA SUPREME CHERRY Other information

each 5 mL teaspoonful contains: calcium 160mg, magnesium 55 mg

• refrigerate after opening to preserve freshness and purity

• protect from freezing
 • keep tightly closed

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

Inactive ingredients

benzyl alcohol, flavor, hydroxyethylcellulose, purified water, saccharin sodium, simethicone emulsion, sorbic acid, sorbitol solution, xanthan gum

package Label

NDC 57896-624-12

GERICARE

GERI-LANTA

supreme

CHERRY FLAVOR

ANTACID with calcium

Fast Acting Relief of:

HEARTBURN

SOUR STOMACH

ACID INDIGESTION

compare to the active ingredients in MYLANTA SUPREME

12 FL OZ (355 mL)

GERI-LANTA SUPREME CHERRY

GERI-LANTA SUPREME CHERRY

calcium carbonate, magnesium hydroxide SUSPENSION

Product Information

Product Type Human otc drug label Item Code (Source) NDC:57896-624
Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
CALCIUM CARBONATE 400 mg
magnesium hydroxide MAGNESIUM CATION 135 mg

Inactive Ingredients

Ingredient Name Strength
BENZYL ALCOHOL
hydroxyethyl cellulose (4000 mpa.s at 1%)
water
SACCHARIN SODIUM DIHYDRATE
DIMETHICONE
sorbic acid
sorbitol
XANTHAN GUM

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:57896-624-12 355 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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