Almacone by Rebel Distributors Corp ALMACONE liquid

Almacone by

Drug Labeling and Warnings

Almacone by is a Otc medication manufactured, distributed, or labeled by Rebel Distributors Corp. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredients

Aluminum Hydroxide 200mg

Magnesium Hydroxide 200mg

PURPOSE

Keep Out of Reach of Children

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

INGREDIENTS AND APPEARANCE

ALMACONE 
almacone liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 21695-840(NDC:0536-0025)
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0) (ALUMINUM HYDROXIDE - UNII:5QB0T2IUN0)	ALUMINUM HYDROXIDE	200 mg  in 5 mL
MAGNESIUM HYDROXIDE (UNII: NBZ3QY004S) (MAGNESIUM HYDROXIDE - UNII:NBZ3QY004S)	MAGNESIUM HYDROXIDE	200 mg  in 5 mL

Inactive Ingredients
Ingredient Name	Strength
BENZYL ALCOHOL (UNII: LKG8494WBH)
BUTYLPARABEN (UNII: 3QPI1U3FV8)
CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
CARBOXYMETHYLCELLULOSE (UNII: 05JZI7B19X)
HYPROMELLOSES (UNII: 3NXW29V3WO)
PROPYLPARABEN (UNII: Z8IX2SC1OH)
WATER (UNII: 059QF0KO0R)
SACCHARIN SODIUM (UNII: SB8ZUX40TY)
SORBITOL (UNII: 506T60A25R)

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

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part331	11/11/2008

Labeler - Rebel Distributors Corp (118802834)

Establishment
Name	Address	ID/FEI	Business Operations
Rebel Distributors Corp		118802834	RELABEL, REPACK