Label: MIRACULOUS HANGOVER- hovenia dulcis thunb liquid

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved drug other

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 April 14, 2022

If you are a consumer or patient please visit this version.

  • Active Ingredient

    HOVENIA DULCIS THUNB. 19%

  • Purpose

    Relieves symptoms of hangover

  • Uses

    Helps relieve headache, fatigue, nausea, vomiting caused from consumption of alcohol

  • Do Not Use

    If you are allergic to any ingredients of this product.

  • When Using This Product

    Do not exceed recommended dosage

  • Stop us and ask a doctor if

    symptoms last for more than 2 weeks

  • Keep out of the reach of children

    Keep out of the reach of children

  • Warnings

    In case of overdose, get medical help or contact a Poison Control Center right away.

  • Directions

    Drink one bottle a day.

  • Other Information

    Store at room temperature.

  • Inactive Ingredients

    PUERARIA MONTANA VAR. LOBATA ROOT, CRATAEGUS PINNATIFIDA WHOLE, CIRSIUM JAPONICUM WHOLE, CITRUS RETICULATA WHOLE, WOLFIPORIA COCOS WHOLE, ATRACTYLODES LANCEA ROOT, SCHISANDRA CHINENSIS WHOLE, RUBUS COREANUS WHOLE, ASTRAGALUS PROPINQUUS ROOT, ZIZIPHUS JUJUBA VAR. INERMIS WHOLE, GLYCYRRHIZA URALENSIS WHOLE, ARTEMISIA CAPILLARIS WHOLE, PRUNUS MUME FLOWER, NASHIPATI, FRUCTOOLIGOSACCHARIDE

  • Label

    Miraculous Hangover Label

  • INGREDIENTS AND APPEARANCE
    MIRACULOUS HANGOVER 
    hovenia dulcis thunb liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:82672-301
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    HOVENIA DULCIS WHOLE (UNII: 1DM83BAP2N) (HOVENIA DULCIS WHOLE - UNII:1DM83BAP2N) HOVENIA DULCIS WHOLE19 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    ATRACTYLODES LANCEA ROOT (UNII: CAZ6282J2O)  
    GLYCYRRHIZA URALENSIS WHOLE (UNII: 8XW1DS8UIR)  
    NASHIPATI (UNII: SHY4TJD066)  
    CRATAEGUS PINNATIFIDA WHOLE (UNII: TMT0402DF6)  
    ASTRAGALUS PROPINQUUS ROOT (UNII: 922OP8YUPF)  
    CIRSIUM JAPONICUM (UNII: WCA3C9S0OM)  
    RUBUS COREANUS WHOLE (UNII: 8X91IS0Z3R)  
    ZIZIPHUS JUJUBA VAR. INERMIS WHOLE (UNII: 7E3OM4YS3V)  
    PUERARIA MONTANA VAR. LOBATA ROOT (UNII: PET93F4I3C)  
    CITRUS RETICULATA WHOLE (UNII: O0OX7CMF92)  
    SCHISANDRA CHINENSIS WHOLE (UNII: RM13YIU944)  
    ARTEMISIA CAPILLARIS WHOLE (UNII: 852FKP35KV)  
    WOLFIPORIA COCOS WHOLE (UNII: Y1I7Z6FF4R)  
    PRUNUS MUME FLOWER (UNII: 2N8872050J)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:82672-301-01110 mL in 1 BOTTLE, GLASS; Type 0: Not a Combination Product04/14/2022
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other04/14/2022
    Labeler - Qingdao Aolixin Sanitary Products Co., Ltd. (711260284)