Label: HAND SANITIZER WIPES- wet wipe swab

  • NDC Code(s): 77046-003-01
  • Packager: ZHEJIANG HUASHUN TECHNOLOGY CO.,LTD
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated March 18, 2024

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  • Use

    To decrease bacteria on the skin.May be used on the face,arms,and body.

  • Warnings

    For external use only. Do not use in eyes. In case of eye contact, rinse eyes with water. Stop use and ask a doctor if skin/eye irritation develops.Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center.

  • Active Ingredient

    Benzalkonium chloride 0.1%.....................................Antibacterial

  • Inactive Ingredient

    Water,Glycerin,Lauryl Glucoside,DMDM Hydantoin,Aloe Barbadensis Leaf Extract,Disodium EDTA,PEG-12 Dimethicone, Panthenol, Chamomilla Recutia(Matricaria) Extract,lodopropynyl Butylcarnate,Tocopheryl Acetate,Allantonin

  • Questions/Comments?

    Call toll free 1-866-748-9990

  • PURPOSE

    Kills 99.99% of germs

  • Directions

    Pull one sheet from soft pack

    clean hands or affected area and discard.

    Close lid after each use to keep wipes fresh

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children

  • package label

    product labeling

  • INGREDIENTS AND APPEARANCE
    HAND SANITIZER WIPES 
    wet wipe swab
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:77046-003
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE0.1 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) 0.05 g  in 100 g
    DECYL GLUCOSIDE (UNII: Z17H97EA6Y) 0.05 g  in 100 g
    ALOE (UNII: V5VD430YW9) 0.05 g  in 100 g
    WATER (UNII: 059QF0KO0R)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T) 0.5 g  in 100 g
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:77046-003-0172 in 1 BAG04/30/2020
    14.15 g in 1 PATCH; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)04/30/2020
    Labeler - ZHEJIANG HUASHUN TECHNOLOGY CO.,LTD (527157837)
    Establishment
    NameAddressID/FEIBusiness Operations
    ZHEJIANG HUASHUN TECHNOLOGY CO., LTD527157837manufacture(77046-003)
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