Label: TOSOWOONG MENS BOOSTER REPAIR SKIN- arbutin 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 July 5, 2013

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

View All Sections
  • ACTIVE INGREDIENT

    arbutin


  • INACTIVE INGREDIENT

    water, alcohol, glyceryl acrylate/acrylic acid copolymer, PVM/MA copolymer, carbomer, portulaca oleracea extract, licorice root extract, morus alba root extract, linaria japonica extract, anthemis nobilis flower extract, asparagus lucidus root extract, coltsfood flower extract, laminaria japonica extract, nelumbo nucifera flower extract, oenanthe javanica extract, hordeum vulgare leaf extract, PEG=60 hydrogenated castor oil, glycerin, betaine, polyglutamic acid, beta-glucan, phenyl trimethicone, ethyl menthane carboxamide, benzophenone-5, triethanolamine, phenoxyethanol, chlorphenesin, caprylyl glycol, ethylhexylglycerin, CI 42090, fragrance


  • PURPOSE

    helps skin whitening


  • KEEP OUT OF REACH OF CHILDREN

    keep out or reach of the children


  • INDICATIONS & USAGE

    take appropriate amount and apply onto all over face  after shaving or facial wash


  • WARNINGS

    avoid contact with eyes



  • DOSAGE & ADMINISTRATION

    for external use only


  • PRINCIPAL DISPLAY PANEL

    package label
  • INGREDIENTS AND APPEARANCE
    TOSOWOONG MENS BOOSTER REPAIR SKIN 
    arbutin liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:55249-1001
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ARBUTIN (UNII: C5INA23HXF) (ARBUTIN - UNII:C5INA23HXF) ARBUTIN1 mg  in 150 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    ALCOHOL (UNII: 3K9958V90M)  
    PORTULACA OLERACEA WHOLE (UNII: D5J3623SV2)  
    GLYCYRRHIZA GLABRA (UNII: 2788Z9758H)  
    MORUS ALBA ROOT BARK (UNII: SV6B76DK9N)  
    CHAMAEMELUM NOBILE FLOWER (UNII: O2T154T6OG)  
    ASPARAGUS COCHINCHINENSIS TUBER (UNII: IZW9WN28HW)  
    PETASITES FRAGRANS (UNII: 7MKJ1A3A9T)  
    NELUMBO NUCIFERA FLOWER (UNII: 61W322NLDV)  
    BARLEY (UNII: 5PWM7YLI7R)  
    POLYOXYL 60 HYDROGENATED CASTOR OIL (UNII: 02NG325BQG)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    BETAINE (UNII: 3SCV180C9W)  
    PHENYL TRIMETHICONE (UNII: DR0K5NOJ4R)  
    ETHYL MENTHANE CARBOXAMIDE (UNII: 6S7S02945H)  
    BENZOPHENONE-5 (UNII: 853Z42ZYAS)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    CHLORPHENESIN (UNII: I670DAL4SZ)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:55249-1001-1150 mL in 1 BOTTLE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other07/05/2013
    Labeler - Mantong (688226855)
    Registrant - Mantong (688226855)
    Establishment
    NameAddressID/FEIBusiness Operations
    Cosmecca Korea Co.,Ltd.688830827manufacture(55249-1001)
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, PubMed, Biochemical Data Summary

More Info on this Drug

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