NON-ALCOHOL FOAMING HAND WASH- benzalkonium chloride 0.10% liquid

Non-Alcohol Foaming Hand Wash by

Drug Labeling and Warnings

Non-Alcohol Foaming Hand Wash by is a Otc medication manufactured, distributed, or labeled by Arkansas Correctional Industries, Allison Corbitt. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

  • DO NOT USE

    Do not use in the eyes

  • STOP USE

    Stop use and ask a doctor if irritation and/or redness occurs or if symptoms persist for more than 72 hours.

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children. If ingested, seek medical attention or contact a Poison Control Center immediately.

  • PURPOSE

    USE for waterless cleansing of hands to decrease soil on the skin

  • QUESTIONS

    To obtain a copy of an SDS or for any questions or concerns, please call (877)635-7213 or visit our website: https://www.acicatalog.com/store/product_detail/753

  • WARNINGS

    WARNINGS

    For external use only

    Do not use in the eyes

    Stop use and ask a doctor if irritation and/or redness occurs or if symptoms persist for more than 72 hours.

    Keep out of reach of children. If ingested, seek medical attention or contact a Poison Control Center immediately.

  • INACTIVE INGREDIENT

    INACTIVE INGREDIENTS

    Water, Laurtrimonium Chloride, Cetrimonium Chloride, Dihydroxyethyl Cocamine Oxide, Fragrance.

  • DOSAGE & ADMINISTRATION

    DIRECTIONS

    Place a palm full (approx. 5 grams) of product in one hand, spread on both hands, and rub into the skin until dry(approximately 1 to 2 minutes).
    Place smaller amount (approx. 2.5 grams) into one hand, spread over both hands to wrist, and rub into the skin until dry(approximately 30 seconds).

  • INDICATIONS & USAGE

    USE for waterless cleansing of hands to decrease soil on the skin

  • PRINCIPAL DISPLAY PANEL

    HAND WAS LABEL

  • INGREDIENTS AND APPEARANCE
    NON-ALCOHOL FOAMING HAND WASH 
    benzalkonium chloride 0.10% liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 78890-001
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE0.1 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    CETRIMONIUM CHLORIDE (UNII: UC9PE95IBP) 0.01 g  in 100 mL
    DIHYDROXYETHYL COCAMINE OXIDE (UNII: 8AR51R3BL5) 0.01 g  in 100 mL
    WATER (UNII: 059QF0KO0R) 99.87 g  in 100 mL
    LAURTRIMONIUM CHLORIDE (UNII: A81MSI0FIC) 0.01 g  in 100 mL
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC: 78890-001-013785 mL in 1 JUG; Type 0: Not a Combination Product06/22/2020
    2NDC: 78890-001-02208198 mL in 1 DRUM; Type 0: Not a Combination Product06/22/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00306/22/2020
    Labeler - Arkansas Correctional Industries (085528712)
    Registrant - Allison Corbitt (085528712)
    Establishment
    NameAddressID/FEIBusiness Operations
    Arkansas Correctional Industries085528712manufacture(78890-001) , pack(78890-001) , label(78890-001)

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