EMETROL CHERRY- phosphorated carbohydrate solution

Emetrol Cherry by

Drug Labeling and Warnings

Emetrol Cherry by is a Otc medication manufactured, distributed, or labeled by Preferred Pharmaceuticals, Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredients

Phosphorated carbohydrate solution*
    *each 5 mL contains:
         3.74 g Total sugar
         21.5 mg Phosphoric acid

Purpose

Upset Stomach Reliever       

Uses

For relief of upset stomach associated with nausea due to overindulgence in food and drink.

Warnings

• This product contains fructose and should not be taken by persons with hereditary fructose intolerance (HFI).

Do not use if you have

• allergic reactions to any of the ingredients in this product

Ask a doctor before use if you have

• diabetes

Stop use and ask a doctor if

• symptoms persist, return or get worse

If pregnant or breast-feeding,

ask a health professional before use.

Keep out of reach of children.

In case of overdose, get medical help or contact a Poison Control Center right away. (1-800-222-1222)

Directions

• For maximum effectiveness never dilute or drink fluids of any kind immediately before or after taking this product
• adults and children 12 years of age and over: one to two tablespoons
• children 2 to under 12: one or two teaspoons
• repeat dose every 15 minutes or until distress subsides
• do not take more than 5 doses in 1 hour without consulting a doctor

Other information

• Store between 20-25ºC (68-77ºF) away from heat and direct light; keep from freezing
• Do not use if printed foil seal under bottle cap is broken or missing

Inactive ingredients

FD&C red no. 40, flavors, glycerin, methylparaben, and purified water.

How Supplied

118cc – 68788-9801-1

Questions or Comments?

call 1-866-337-4500

Distributed By

WellSpring Pharmaceutical Corporation
Sarasota, FL 34243 USA
(c) WellSpring 2009

Relabeled By Preferred Pharmaceuticals, Inc

PACKAGE LABEL

INGREDIENTS AND APPEARANCE

EMETROL CHERRY 
phosphorated carbohydrate solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 68788-9801(NDC:65197-201)
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SUCROSE (UNII: C151H8M554) (SUCROSE - UNII:C151H8M554)	SUCROSE	3.74 g  in 5 mL
PHOSPHORIC ACID (UNII: E4GA8884NN) (PHOSPHORIC ACID - UNII:E4GA8884NN)	PHOSPHORIC ACID	21.5 mg  in 5 mL

Inactive Ingredients
Ingredient Name	Strength
FD&C RED NO. 40 (UNII: WZB9127XOA)
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
METHYLPARABEN (UNII: A2I8C7HI9T)

Product Characteristics
Color	RED (Red)	Score
Shape		Size
Flavor	CHERRY	Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 68788-9801-1	118 mL in 1 BOTTLE

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Unapproved drug other		04/23/2012

Labeler - Preferred Pharmaceuticals, Inc (791119022)

Establishment
Name	Address	ID/FEI	Business Operations
Preferred Pharmaceuticals, Inc		791119022	RELABEL(68788-9801)