EMETROL CHERRY- phosphorated carbohydrate solution 
WellSpring Pharmaceutical Corporation

Disclaimer: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

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Emetrol

Active ingredients (per 5mL)

Dextrose (glucose) 1.87g

Levulose (fructose) 1.87g

Phosphoric acid 21.5mg

Purpose

Upset Stomach Reliever       

Uses

for relief of upset stomach associated with nausea

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
repeat dose every 15 minutes or until distress subsides
do not take more than 5 doses in 1 hour without consulting a doctor
measure only with dosing cup provided. Dosing cup to be used with product only. Do not use with other products.
mL = milliliters

Age

Dose

Adults and children 12 years of age and over

15 mL or 30 mL

Children 2 to under 12 years of age

5 mL or 10 mL

Other information

Store between 15-30ºC (59-86ºF) 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.

Questions or Comments?

call 1-844-241-5454

Distributed By

© 2020 WellSpring Pharmaceutical Corporation
Sarasota, Florida 34243 USA
Made in USA

PACKAGE LABEL

NON DROWSY Emetrol Rapid Nausea Relief 

EMETROL CHERRY 
phosphorated carbohydrate solution
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:65197-201
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
DEXTROSE, UNSPECIFIED FORM (UNII: IY9XDZ35W2) (DEXTROSE, UNSPECIFIED FORM - UNII:IY9XDZ35W2) DEXTROSE, UNSPECIFIED FORM1.87 g  in 5 mL
FRUCTOSE (UNII: 6YSS42VSEV) (FRUCTOSE - UNII:6YSS42VSEV) FRUCTOSE1.87 g  in 5 mL
PHOSPHORIC ACID (UNII: E4GA8884NN) (PHOSPHORIC ACID - UNII:E4GA8884NN) PHOSPHORIC ACID21.5 mg  in 5 mL
Inactive Ingredients
Ingredient NameStrength
FD&C RED NO. 40 (UNII: WZB9127XOA)  
WATER (UNII: 059QF0KO0R)  
GLYCERIN (UNII: PDC6A3C0OX)  
METHYLPARABEN (UNII: A2I8C7HI9T)  
Product Characteristics
ColorRED (Red) Score    
ShapeSize
FlavorCHERRYImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:65197-201-041 in 1 CARTON06/24/2009
1118 mL in 1 BOTTLE; Type 0: Not a Combination Product
2NDC:65197-201-06133 mL in 1 BOTTLE; Type 0: Not a Combination Product11/01/2018
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
Unapproved drug other06/24/2009
Labeler - WellSpring Pharmaceutical Corporation (110999054)

Revised: 12/2021
Document Id: ae999e34-0f0c-4eb2-a1d1-a715cc7ba961
Set id: a8469128-592a-4682-82c7-4d2a6f97a998
Version: 29
Effective Time: 20211203
 
WellSpring Pharmaceutical Corporation