LIQUFRUTA- guaifenesin syrup

Liqufruta by

Drug Labeling and Warnings

Liqufruta by is a Otc medication manufactured, distributed, or labeled by Alston Garrard & Co, Pharmaserve (North West) Ltd . Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

GUAIFENESIN 50 MG/TEASPOON (5ML)

PURPOSE

EXPECTORANT -HELPS LOOSEN PHLEGM (MUCUS) AND THIN BRONCHIAL SECRETIONS TO MAKE COUGH MORE PRODUCTIVE

KEEP OUT OF REACH OF CHILDREN

Keep out reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.

INDICATIONS & USAGE

Loosens and Relieves Chest congestion

WARNINGS

Ask a doctor before use if you have a cough that last or it is chronic such as occurs with smoking, asthma, chronic Bronchitis or emphysema. Stop use and ask doctor if a cough lasts for more than 7 days comes back or occurs when fever, rash or persistent headache. A persistent cough may be a sign of a serious condition.
If pregnant of breast-feeding, ask a health professional before use.

DOSAGE & ADMINISTRATION

do not take more than 6 doses in a 24-hour period
AGE ......................................................DOSE
Adults and Children 12 years and over .......2-4 teaspoonfuls(tsp) every 4 hours
Children 6 years and under 12 years......... 1-2 teaspoonfuls(tsp) every 4 hours
Children 2 years and under 6 years........... 1/2-1 teaspoonfuls(tsp) every 4 hours
Under 2 years ........................................ask a doctor

INACTIVE INGREDIENT

Purified water, natural garlic oil,caramel, high fructose sucrose, menthol, ethanol, sodium citrate, citric acid, sodium benzoate, acetic acid

QUESTIONS

OTHER Information
Shake well Before Use
store at room temp (59F-86)


imported and Distributed by:
Bedessee Imports Ltd.
Brooklyn, NY USA 11208
1-888-BEDESSEE
416-292-2400

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

LIQUFRUTA 
guaifenesin syrup

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 75939-9876
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
GUAIFENESIN (UNII: 495W7451VQ) (GUAIFENESIN - UNII:495W7451VQ)	GUAIFENESIN	50 mg  in 5 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
ALCOHOL (UNII: 3K9958V90M)
SODIUM CITRATE (UNII: 1Q73Q2JULR)
GARLIC OIL (UNII: 4WG8U28833)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
HIGH FRUCTOSE CORN SYRUP (UNII: XY6UN3QB6S)
SODIUM BENZOATE (UNII: OJ245FE5EU)
CARAMEL (UNII: T9D99G2B1R)
MENTHOL (UNII: L7T10EIP3A)
ACETIC ACID (UNII: Q40Q9N063P)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 75939-9876-2	200 mL in 1 BOTTLE, PLASTIC

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part341	01/01/2011

Labeler - Alston Garrard & Co (735697570)

Registrant - Alston Garrard & Co (735697570)

Establishment
Name	Address	ID/FEI	Business Operations
Pharmaserve (North West) Ltd		210141282	manufacture