Label: MEDEX HAND SANITIZER- ethyl alcohol gel

  • NDC Code(s): 60717-802-01, 60717-802-02, 60717-802-04, 60717-802-06, view more
    60717-802-08, 60717-802-12, 60717-802-16
  • Packager: RNA PHARMA, LLC
  • 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 April 7, 2020

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

  • ACTIVE INGREDIENT

    active ingredientactive ingredientactive ingredientactive ingredientactive ingredientactive ingredientactive ingredient

  • INACTIVE INGREDIENT

    inactive ingredients

  • DOSAGE & ADMINISTRATION

    dosage & administration

  • WARNINGS

    warnings

  • INDICATIONS & USAGE

    indication & usage

  • KEEP OUT OF REACH OF CHILDREN

    keep out reach of children

  • PURPOSE

    purpose

  • PRINCIPAL DISPLAY PANEL

    package principalpackage label principalpackage label principalpackage label principalpackage label principalpackage label principalpackage label principal

  • INGREDIENTS AND APPEARANCE
    MEDEX HAND SANITIZER 
    ethyl alcohol gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:60717-802
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL0.62 g
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)  
    CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
    ISOPROPYL ALCOHOL (UNII: ND2M416302)  
    AMINOMETHYLPROPANOL (UNII: LU49E6626Q)  
    CARBOMER INTERPOLYMER TYPE B (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 132584PQMO)  
    ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    Product Characteristics
    Color    Score    
    ShapeROUNDSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:60717-802-041 in 1 BOTTLE; Type 0: Not a Combination Product03/19/2020
    2NDC:60717-802-081 in 1 BOTTLE, PUMP; Type 0: Not a Combination Product03/19/2020
    3NDC:60717-802-121 in 1 BOTTLE, PUMP; Type 0: Not a Combination Product03/19/2020
    4NDC:60717-802-021 in 1 BOTTLE; Type 0: Not a Combination Product03/19/2020
    5NDC:60717-802-061 in 1 BOTTLE, PUMP; Type 0: Not a Combination Product03/19/2020
    6NDC:60717-802-011 in 1 BOTTLE; Type 0: Not a Combination Product03/19/2020
    7NDC:60717-802-161 in 1 BOTTLE, PUMP; Type 0: Not a Combination Product04/07/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333E03/19/2020
    Labeler - RNA PHARMA, LLC (079103999)
    Establishment
    NameAddressID/FEIBusiness Operations
    RNA PHARMA, LLC079103999manufacture(60717-802)