Label: UP (AND) UP GREEN APPLE SCENT- chloroxylenol soap

  • 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 June 30, 2016

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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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