Label: CLEANCOM- sanitizing wipe cloth

  • NDC Code(s): 80436-005-01, 80436-005-02
  • Packager: RMT Global Partners, LLC
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated October 10, 2024

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  • Active Ingredient(s)

    Benzalkonium Chloride 0.1%.........-: oa Antimicrobial

  • Purpose

    Antimicrobial

  • Use

    For hand sanitizing to decrease bacteria on the skin. Recommended for repeated use

  • Warnings

    Warnings For external use only
    When using this, avoid contact with the eyes. In case of eye contact, flush eyes with water.

  • WHEN USING

    Do not use in or near the eyes. In case of contact with eyes flush thoroughly with water.

  • STOP USE

    Stop use and ask a doctor if irritation or redness develops, —
    or if the condition persists for more than 72 hours.

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children. If swallowed, get medical
    help or contact a Poison Control Center right away.

  • Directions

    Apply to hands, Allow skin to dry without wiping

  • Inactive ingredients

    Water, Ethyl Alcohol, Coamidoporpyl PG-
    Dimonium, Chloride Phosphate, Linear Alcohol Ethoxylate, Fragrance

  • Package Label - Principal Display Panel

    Sanitizer 200 CleancomNDC: 80436-005-01

  • INGREDIENTS AND APPEARANCE
    CLEANCOM 
    sanitizing wipe cloth
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:80436-005
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE0.01 mg
    Inactive Ingredients
    Ingredient NameStrength
    COCAMIDOPROPYL PG-DIMONIUM CHLORIDE PHOSPHATE (UNII: H2KVQ74JM4)  
    ALCOHOL (UNII: 3K9958V90M)  
    1-ETHOXYUNDECANE (UNII: R428J6A8Q2)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:80436-005-01200 in 1 BAG; Type 0: Not a Combination Product01/17/2024
    2NDC:80436-005-021200 in 1 CASE; Type 0: Not a Combination Product01/17/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00301/17/2024
    Labeler - RMT Global Partners, LLC (060652584)
    Establishment
    NameAddressID/FEIBusiness Operations
    Yangzhou Suxiang Medical Instrument Co., Ltd543387280manufacture(80436-005)
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