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

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Almacone

Rebel Distributors Corp

Almacone Drug Facts


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Active ingredients

Aluminum Hydroxide 200mg

Magnesium Hydroxide 200mg

Purpose

Keep Out of Reach of Children

Almacone Uses

Use(s)

Enter section text here

Uses relieves

• heartburn

• acid indigestion

• sour stomach

• gas associated with these conditions

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 syptoms last more than 2 weeks.

KEEP OUT OF REACH OF CHILDREN.

TAMPER EVIDENT: DO NOT USE IF IMPRINTED SAFETY SEAL UNDER CAP IS BROKEN OR MISSING

Directions

Shake well before use. Do not take more than 24 teaspoonful in 24 hours or use the maximum dosage for more than 2 weeks. Adults and children 12 years and older: take 2 to 4 teaspoonsfuls between meals, at bedtime, or as directed by a doctor.

Children under 12 years: ask a doctor.

Other Information

Each 5 mL teaspoon contains:

magnesium 25 mg, sodium 1 mg. Store at room temperature. Protect from freezing. Keep tighly closed.

Inactive ingredients

Benzoyl alcohol, butylparaben, carboxy methylcellulose sodium, flavor, hypromelloses, microcrystalline cellulose, propylparaben, purified water, saccharin sodium, sorbitol solution.

How Supplied

Almacone (antacid) is supplied in 12 oz. bottles NDC 21695-840-12

Questions or comments?

Call 1-800-645-2158, 9 am - 5 pm EST, Monday-Friday.

Distributed by:

Rugby Laboratories

Duluth, GA 30097

Repackaged by:

Rebel Distributors Corp

Thousand Oaks, CA 91320

Package/Label Principal Display Panel

Almacone

Almacone

Almacone LIQUID

Product Information

Product Type Human otc drug label Item Code (Source) NDC:21695-840(NDC:0536-0025)
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

Inactive Ingredients

Ingredient Name Strength
BENZYL ALCOHOL
BUTYLPARABEN
cellulose, microcrystalline
CARBOXYMETHYLCELLULOSE
HYPROMELLOSES
PROPYLPARABEN
water
saccharin sodium
sorbitol

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:21695-840-12 355 in 1 BOTTLE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part331 2008-11-11


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