Label: HAND SANITIZER GEL(AG)- hand sanitizer gel

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved homeopathic

DISCLAIMER: This homeopathic product has not been evaluated by the Food and Drug Administration for safety or efficacy. FDA is not aware of scientific evidence to support homeopathy as effective.

Drug Label Information

Updated May 12, 2020

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

  • DOSAGE & ADMINISTRATION

    Keep tightly closed in a cool.dark,dry place.

  • INACTIVE INGREDIENT

    Vitamin

    Glyceryl stearate

    Hydroxyethyl cellulose

    Essence

  • INDICATIONS & USAGE

    jput Proper Amount Of The Hand Sanitizer lnto Your Palm And Gently Rub it Over Your Palms,ths Back Of Your Hands,fingers And The Spaces Between your Fingers,rub Your Hands Together Continuously Until They Are Dry

  • ACTIVE INGREDIENT

    Silver ions

  • KEEP OUT OF REACH OF CHILDREN

    keep out of reach of children

  • PURPOSE

    Disinfection
    Sterilization
    No Rinseing

  • WARNINGS

    1.This product is for external use only,Do not take it internally.

    2.Keep out of reach of children.

  • PRINCIPAL DISPLAY PANEL

    label

  • INGREDIENTS AND APPEARANCE
    HAND SANITIZER GEL(AG) 
    hand sanitizer gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:54039-001
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SILVER CATION (UNII: 57N7B0K90A) (SILVER CATION - UNII:57N7B0K90A) SILVER CATION10 g  in 500 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  
    HYDROXYETHYL CELLULOSE, UNSPECIFIED (UNII: T4V6TWG28D)  
    .ALPHA.-TOCOPHEROL (UNII: H4N855PNZ1)  
    METHYL BENZOATE (UNII: 6618K1VJ9T)  
    Product Characteristics
    Color    Score    
    ShapeSize
    FlavorImprint Code SILVERELF
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:54039-001-01500 mL in 1 BOTTLE; Type 0: Not a Combination Product05/11/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved homeopathic05/11/2020
    Labeler - Anhui Wanxing Industry Co.,Ltd. (540397995)
    Establishment
    NameAddressID/FEIBusiness Operations
    Anhui Wanxing Industry Co.,Ltd.540397995manufacture(54039-001)