ANTI NAUSEA LIQUID- phosphorated carbohydrate solution 
TOPCO ASSOCIATES LLC

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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Anti Nausea Liquid 4FL OZ (118mL) Cherry Flavor

Active ingredients (per 5 mL)

Dextrose (glucose) 1.87 g

Levulose (fructose) 1.87 g

Purpose

Upset Stomach Reliever       

Uses

For relief of upset stomach associated with nausea.

Warnings

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

  1. age
  1. dose
  1. adults and children 12 years of age and over
  1. 15 mL or 30 mL
  1. children 2 to under 12 years of age
  1. 5 ml or 10 mL

Other information

Inactive ingredients

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

Questions or Comments?

1-888-423-0139

TopCare ®health™

Compare to Emetrol ®Active Ingredients*

Anti - Nausea Liquid

Relief from Nausea due to Upset Stomach

Safe and Effective for Children and Adults

FREE FROM:

CHERRY FLAVOR

Naturally and Artificially Flavored

IMPORTANT :Keep this carton for future reference on full labeling.

DISTRIBUTED BY TOPCO ASSOCIATES LLC

ELK GROVE VILLAGE IL 60007

©TOPCO RARA0318

QUESTIONS? 1-888-423-0139

topcare@topco.comwww.topcarebrand.com

This TopCare ®product is laboratory tested to guarantee its highest quality.

Your total satisfaction is guaranteed.

This product is not manufactured or distributed by Wellspring Pharmaceutical Corporation., owner of the registered trademark Emetrol ®.

PACKAGE LABEL

TopCare health Anti-Nausea Liquid 

ANTI NAUSEA LIQUID 
phosphorated carbohydrate solution
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:36800-708
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
DEXTROSE, UNSPECIFIED FORM (UNII: IY9XDZ35W2) (ANHYDROUS DEXTROSE - UNII:5SL0G7R0OK) 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)  
GLYCERIN (UNII: PDC6A3C0OX)  
METHYLPARABEN (UNII: A2I8C7HI9T)  
WATER (UNII: 059QF0KO0R)  
Product Characteristics
Colorred (Red) Score    
ShapeSize
FlavorCHERRYImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:36800-708-041 in 1 CARTON05/14/2018
1118 mL in 1 BOTTLE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other05/14/2018
Labeler - TOPCO ASSOCIATES LLC (006935977)

Revised: 11/2025
Document Id: 433baaad-076b-9bc3-e063-6394a90a26f0
Set id: fd0e8feb-89b5-42ff-806a-55b7473cf587
Version: 8
Effective Time: 20251110
 
TOPCO ASSOCIATES LLC