Label: MOXIE HAND WIPES- benzalkonium chloride cloth

  • NDC Code(s): 77720-035-01, 77720-035-02
  • Packager: Skaffles Group
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved drug other

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Drug Label Information

Updated May 15, 2024

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  • Active Ingredient

    Benzalkonium Chloride (0.13%)

  • Purpose

    Antibacterial

  • DRUG FACTS

  • Use

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

    For external use only.

  • Do not use

    • If you are allergic to any of the ingredients
    • In the eyes. If contact occurs, rinse thoroughly with water.

    Discontinue use if irritation and redness develop.If condition persists for more than 72 hours consult a doctor.

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

  • Directions

    • Adults and children 2 yrs and over, apply to hands and allow skin to dry without wiping.
    • Children under 2, ask doctor before use.
  • Inactive Ingredients

    Water, Phenoxyethanol, Potassium Sorbate, Sodum Benzoate, Cetylpyridinium Chloride, Disodium Cocoamphodiacetate, Disodium EDTA, PEG-8 Dimethicone, Aloe Barbadensis Leaf Juice, Chamomilla Recutita (Matricacria), Flower Extract, Quaternium-52, Citric Acid, PEG075 Lanolin.

  • 888-251-009

  • Principal Display Panel

    Moxie

    ANTIBACTERIAL HAND WIPES

    Kills 99.9% of most comon gems

    Moisturizes with Aloe

    Unscented

    6.5 in x 4.5 in (16.5 cm x 11.4 cm)

    1CT

    Distributed by: Lowe's Home Centers LLC,

    Mooresville NC 28117 888-251-009

    MADE IN CHINA

    See outer packaging for manufacturing date & expiration date

    Principal DP

  • INGREDIENTS AND APPEARANCE
    MOXIE HAND WIPES 
    benzalkonium chloride cloth
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:77720-035
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE0.13 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    PEG-75 LANOLIN (UNII: 09179OX7TB)  
    POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
    CETYLPYRIDINIUM CHLORIDE (UNII: D9OM4SK49P)  
    QUATERNIUM-52 (UNII: 588EQF3H1P)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    MATRICARIA CHAMOMILLA FLOWERING TOP OIL (UNII: SA8AR2W4ER)  
    PEG-8 DIMETHICONE (UNII: GIA7T764OD)  
    WATER (UNII: 059QF0KO0R)  
    DISODIUM COCOAMPHODIACETATE (UNII: 18L9G3U51M)  
    EDETATE DISODIUM (UNII: 7FLD91C86K)  
    SODIUM BENZOATE (UNII: OJ245FE5EU)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    Product Characteristics
    Color    Score    
    ShapeRECTANGLESize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:77720-035-011 mL in 1 POUCH; Type 0: Not a Combination Product05/06/2024
    2NDC:77720-035-0250 mL in 1 POUCH; Type 0: Not a Combination Product05/06/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other05/06/2024
    Labeler - Skaffles Group (831115642)
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