UP (AND) UP GREEN APPLE SCENT (CHLOROXYLENOL) SOAP [SUN PRODUCTS CORPORATION]

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  • UP (AND) UP GREEN APPLE SCENT (CHLOROXYLENOL) SOAP [SUN PRODUCTS CORPORATION]

UP (AND) UP GREEN APPLE SCENT (CHLOROXYLENOL) SOAP [SUN PRODUCTS CORPORATION]
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NDC 63691-029-10, 63691-029-30
Set ID 27fa2840-adae-045a-e054-00144ff8d46c
Category HUMAN OTC DRUG LABEL
Packager Sun Products Corporation
Generic Name
Product Class
Product Number
Application Number PART333E
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  • Active Ingredient

    Chloroxylenol 0.30%

  • Use

    for handwashing to decrease bacteria on the skin

  • Warnings

    For external use only

  • KEEP OUT OF REACH OF CHILDREN

    In case of accidental ingestion, drink a glass of water to dilute. If eye contact occurs, rinse thoroughly with water.

  • DOSAGE & ADMINISTRATION

    Directions wet hands and forearms. Apply 5 ml or palmful to hands and forearms. Scrub thoroughly for 30 sec. and rinse.

  • Purpose

    Antibacterial hand soap

  • Inactive ingredients

    Water, Sodium Laureth Sulfate, Sodium Dodecylbenzenesulfonate, Sodium Chloride, Alcohol Denat., Sodium Xylenesulfonate, Soidum Lauryl Sulfate, Tetrasodium EDTA, Benzisothiazolinone, Methylisothiazolinone, Methylchloroisothiazolinone, Fragrance, FD&C Yello No. 5, FD&C Blue No. 1

  • QUESTIONS

    Questions? 1-800-910-6874

  • Target 60oz GAAB LDU 690004755_690005736-page-001.jpg Target 24oz GAAB LDU 4900008630_4900008631-page-001.jpg

    Target 24 ozUP(and)UP GAAB

  • INGREDIENTS AND APPEARANCE
    UP (AND) UP GREEN APPLE SCENT 
    chloroxylenol soap
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:63691-029
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CHLOROXYLENOL (UNII: 0F32U78V2Q) (CHLOROXYLENOL - UNII:0F32U78V2Q) CHLOROXYLENOL0.3 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM LAURETH SULFATE (UNII: BPV390UAP0)  
    SODIUM XYLENESULFONATE (UNII: G4LZF950UR)  
    EDETATE SODIUM (UNII: MP1J8420LU)  
    BENZISOTHIAZOLINONE (UNII: HRA0F1A4R3)  
    WATER (UNII: 059QF0KO0R)  
    SODIUM DODECYLBENZENESULFONATE (UNII: 554127163Y)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    ALCOHOL (UNII: 3K9958V90M)  
    SODIUM LAURYL SULFATE (UNII: 368GB5141J)  
    METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)  
    METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)  
    FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:63691-029-301774 mL in 1 BOTTLE; Type 0: Not a Combination Product12/01/2015
    2NDC:63691-029-10709 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product04/30/2016
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333E11/30/2015
    Labeler - Sun Products Corporation (070931480)
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