Label: NAUSEA RELIEF (dextrose (glucose), levulose- fructose, phosphoric acid 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 27, 2024

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  • Active ingredients (per 5 mL)

    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

    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 = 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 at 20-25°C (68-77°F) away from heat and direct light; keep from freezing.
    do not use if printed neckband is broken or missing
  • Inactive ingredients

    FD&C red no. 40 aluminum lake, flavor, glycerin, methylparaben, purified water

  • Questions or comments?

    1-800-719-9260

  • Package/Label Principal Display Panel

    Compare to the active ingredients of Emetrol®

    nausea relief

    dextrose (glucose) 1.87 g

    levulose (fructose) 1.87 g

    phosphoric acid 21.5 mg

    for children and adults

    relief for nausea due to upset stomach

    no antihistamines

    no aspirin

    no alcohol

    no caffeine

    cherry flavor

    4 FL OZ (118 mL)

    291-83-nausea-relief.jpg
  • INGREDIENTS AND APPEARANCE
    NAUSEA RELIEF 
    dextrose (glucose), levulose (fructose), phosphoric acid solution
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11822-0401
    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 (clear) Score    
    ShapeSize
    FlavorCHERRYImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:11822-0401-11 in 1 CARTON11/04/201402/28/2025
    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 other11/04/201402/28/2025
    Labeler - Rite Aid Corporation (014578892)