Label: RESET U- hovenia dulcis thunb. liquid

  • NDC Code(s): 82229-001-01, 82229-001-02, 82229-001-03, 82229-001-04, view more
    82229-001-05, 82229-001-06
  • Packager: DOCTOR CARE
  • 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 November 17, 2023

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

  • Active ingredient

    HOVENIA DULCIS THUNB. 19%

  • Purpose

    Hangover

  • Uses

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

  • Warnings

  • When using this product,

    do not exceed recommended dosage

  • Stop use and ask a doctor if

    symptoms last for more than 2 weeks

  • Keep out of reach of children

    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

  • Package Label

    82229-001-01

    82229-001-02

    82229-001-03

    82229-001-04

    82229-001-05

    82229-001-06

  • INGREDIENTS AND APPEARANCE
    RESET U 
    hovenia dulcis thunb. liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:82229-001
    Route of AdministrationTOPICAL
    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
    SCHISANDRA CHINENSIS WHOLE (UNII: RM13YIU944)  
    ARTEMISIA CAPILLARIS WHOLE (UNII: 852FKP35KV)  
    NASHIPATI (UNII: SHY4TJD066)  
    PUERARIA MONTANA VAR. LOBATA ROOT (UNII: PET93F4I3C)  
    CRATAEGUS PINNATIFIDA WHOLE (UNII: TMT0402DF6)  
    CITRUS RETICULATA WHOLE (UNII: O0OX7CMF92)  
    WOLFIPORIA COCOS WHOLE (UNII: Y1I7Z6FF4R)  
    ASTRAGALUS PROPINQUUS ROOT (UNII: 922OP8YUPF)  
    PRUNUS MUME FLOWER (UNII: 2N8872050J)  
    ATRACTYLODES LANCEA ROOT (UNII: CAZ6282J2O)  
    CIRSIUM JAPONICUM (UNII: WCA3C9S0OM)  
    RUBUS COREANUS WHOLE (UNII: 8X91IS0Z3R)  
    ZIZIPHUS JUJUBA VAR. INERMIS WHOLE (UNII: 7E3OM4YS3V)  
    GLYCYRRHIZA URALENSIS WHOLE (UNII: 8XW1DS8UIR)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:82229-001-0175 mL in 1 BOTTLE, GLASS; Type 0: Not a Combination Product09/16/202110/21/2022
    2NDC:82229-001-0217 mL in 1 POUCH; Type 0: Not a Combination Product09/16/202110/21/2022
    3NDC:82229-001-0320 mL in 1 POUCH; Type 0: Not a Combination Product09/16/202110/21/2022
    4NDC:82229-001-05110 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product09/16/202110/21/2022
    5NDC:82229-001-06120 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product09/16/202110/21/2022
    6NDC:82229-001-04100 mL in 1 BOTTLE, GLASS; Type 0: Not a Combination Product09/16/2021
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other09/16/2021
    Labeler - DOCTOR CARE (695376548)
    Registrant - DOCTOR CARE (695376548)
    Establishment
    NameAddressID/FEIBusiness Operations
    DOCTOR CARE695376548manufacture(82229-001)