Label: NUVOMED ANTIBACTERIAL WET WIPES- benzalkonium chloride cloth

  • NDC Code(s): 76635-005-01, 76635-005-02, 76635-005-03
  • Packager: Hangzhou Glamcos Biotech CO.,LTD
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated November 23, 2023

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  • SPL UNCLASSIFIED SECTION

    Drug Facts

  • Active Ingredient(s)

    Benzalkonium Chloride 0.3%

  • Purpose

    Antiseptic

  • Use

    Use for hand-washing to decrease bacteria on the skin when water is not available.

  • Warnings

    Keep away from fire and flames.For external use only.

  • Do not use

    Do not use on open or broken skin.If contact occurs,rinse eyes thoroughly with water.

  • WHEN USING

    When using this product ,do not get in eyes.

  • STOP USE

    Stop use and ask a doctor if irritation and redness develop.

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children.If swallowed,get medical help or contact poison control center right away.

  • Directions

    Wet hands thoroughly with product and allow to dry 20-30 seconds.Do not dry or wipe when finished.

  • Other information

    The espiry date is stated on the packaging.Store at -20℃ to+30℃,away from sunlight.

  • Inactive ingredients

    Water，Propylene Glycol，DidecyldimoniumChloride ，Phenoxyethanol， Chlorphenesin.

  • Package Label - Principal Display Panel

    label-15 wipeslabel-60 wipeslabel-75 wipes

  • INGREDIENTS AND APPEARANCE
    NUVOMED ANTIBACTERIAL WET WIPES 
    benzalkonium chloride cloth
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:76635-005
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE0.3 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    DIDECYLDIMONIUM CHLORIDE (UNII: JXN40O9Y9B)  
    WATER (UNII: 059QF0KO0R)  
    CHLORPHENESIN (UNII: I670DAL4SZ)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:76635-005-0155 g in 1 BAG; Type 0: Not a Combination Product05/23/2020
    2NDC:76635-005-02218 g in 1 BAG; Type 0: Not a Combination Product05/23/2020
    3NDC:76635-005-03290 g in 1 BAG; Type 0: Not a Combination Product05/23/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)05/23/2020
    Labeler - Hangzhou Glamcos Biotech CO.,LTD (554476017)
    Registrant - Hangzhou Glamcos Biotech CO.,LTD (554476017)
    Establishment
    NameAddressID/FEIBusiness Operations
    Hangzhou Glamcos Biotech CO.,LTD554476017manufacture(76635-005)
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