Label: ANTI NAUSEA LIQUID- phosphorated carbohydrate solution

  • Category: HUMAN OTC DRUG LABEL

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.

Drug Label Information

Updated November 6, 2024

If you are a healthcare professional or from the pharmaceutical industry please visit this version.

View All Sections
  • Active ingredients (per 5 mL)

    Dextrose (glucose) 1.87 g

    Levulose (fructose) 1.87 g

     
    Phosphoric acid 21.5 mg
  • 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 this product only. Do not use with other products.
    •
    mL= milliliter
     
    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 at room temperature away from heat and direct light; keep from freezing
    •
    Do not use if printed seal under cap is broken or missing
  • Inactive ingredients

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

  • Questions or Comments?

    1-888-423-0139

  • SPL UNCLASSIFIED SECTION

    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:

    •
    Antihistamines
    •
    Salicylates
    •
    Alcohol
    •
    Caffeine

    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 

  • INGREDIENTS AND APPEARANCE
    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)
View All Sections

Find additional resources

(also available in the left menu)

Safety

Report Adverse Events, FDA Safety Recalls, Presence in Breast Milk

Related Resources

Medline Plus, Clinical Trials

More Info on this Drug

Get Label RSS Feed, View NDC Code(s)NEW!