Label: PETER PAN ALCOHOL FREE FOAMING HAND SANITIZER- benzalkonium chloride lotion

  • 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 January 20, 2011

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

  • Active Ingredients

    E0.13% Benzylkonium Chloride

  • INDICATIONS & USAGE


    Requires no water or towels.  Apply small amount to hands and rub lightly until dry.
  • WARNINGS

    Safety: Avoid contact with  Eyes, should this occur  rinse immediately with clean warm water.

    Caution: Use on hands only.

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children.

  • PURPOSE

    Kills 99.9% Bacteria

  • DOSAGE & ADMINISTRATION

    Requires no water or towels.

    Apply small amount to hands and rub lightly until dry.

  • INACTIVE INGREDIENT

    Aqua, Polysorbate 40, Aloe Barbadensis, Parfum

  • PRINCIPAL DISPLAY PANEL

    Peter Pan Label 


  • INGREDIENTS AND APPEARANCE
    PETER PAN  ALCOHOL FREE FOAMING HAND SANITIZER
    benzalkonium chloride lotion
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:52305-400
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    Benzalkonium Chloride (UNII: F5UM2KM3W7) (Benzalkonium - UNII:7N6JUD5X6Y) Benzalkonium Chloride.364 g  in 280 mL
    Inactive Ingredients
    Ingredient NameStrength
    Water (UNII: 059QF0KO0R)  
    POLYSORBATE 40 (UNII: STI11B5A2X)  
    ALOE VERA FLOWER (UNII: 575DY8C1ER)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:52305-400-20280 mL in 1 BOTTLE, PUMP
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A01/20/2011
    Labeler - Freshorize, Ltd. (424168503)
    Registrant - Freshorize, Ltd. (424168503)
    Establishment
    NameAddressID/FEIBusiness Operations
    Freshorize, Ltd.424168503manufacture