Label: JEJUON DAILYCARE HANDWASH- benzalkonium chloride liquid

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph not final

DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Drug Label Information

Updated May 7, 2020

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  • PRINCIPAL DISPLAY PANEL

    handwash tube

  • INGREDIENTS AND APPEARANCE
    JEJUON DAILYCARE HANDWASH 
    benzalkonium chloride liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:76744-150
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE0.5 g  in 50 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX)  
    SODIUM LAURYL SULFATE (UNII: 368GB5141J)  
    LAVANDULA ANGUSTIFOLIA FLOWERING TOP (UNII: 9YT4B71U8P)  
    LIME OIL (UNII: UZH29XGA8G)  
    TURMERIC (UNII: 856YO1Z64F)  
    HYALURONATE SODIUM (UNII: YSE9PPT4TH)  
    JUNIPERUS DEPPEANA WOOD OIL (UNII: 4739QA5686)  
    CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    TANGERINE (UNII: KH3E3096OO)  
    NELUMBO NUCIFERA LEAF (UNII: 60C608DPVT)  
    ROSEMARY (UNII: IJ67X351P9)  
    ORANGE OIL (UNII: AKN3KSD11B)  
    XANTHAN GUM (UNII: TTV12P4NEE)  
    1,2-HEXANEDIOL (UNII: TR046Y3K1G)  
    HEXYLENE GLYCOL (UNII: KEH0A3F75J)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    WATER (UNII: 059QF0KO0R)  
    DISODIUM COCOAMPHODIACETATE (UNII: 18L9G3U51M)  
    POTASSIUM COCOYL GLYCINATE (UNII: WZ70FUF22U)  
    EUCALYPTUS OIL (UNII: 2R04ONI662)  
    LAVANDIN OIL (UNII: 9RES347CKG)  
    BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:76744-150-0150 mL in 1 TUBE; Type 0: Not a Combination Product05/08/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333E05/08/2020
    Labeler - Korea Beauty Industry Development Institute Co.,Ltd. (690485683)
    Registrant - Korea Beauty Industry Development Institute Co.,Ltd. (690485683)
    Establishment
    NameAddressID/FEIBusiness Operations
    Korea Beauty Industry Development Institute Co.,Ltd.695538825manufacture(76744-150)