Label: LITTLE ME SANITIZER- little me sanitizer spray spray

  • NDC Code(s): 76860-006-01
  • Packager: Taizhou Huangyan Liweir Cosmetic Technology Ltd.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated April 16, 2024

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  • SPL UNCLASSIFIED SECTION

    NA

  • Active Ingredient(s)

    Benzalkonium Chloride 0.13%

  • Purpose

    Antibacterial Agent

  • Use

    for hand-washing to decrease bacteria on the skin, only when water is not available

  • Warnings

    For external use only

  • WHEN USING

    When using the product do not get into eyes. If contact occurs, rinse thoroughly with water.

  • STOP USE

    Stop use and ask a doctor if irritation occurs or rash develops and continues 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

    adults and children 2 years and over

    - apply to hands

    - allow skin to dry without wiping

    children under 2 years

    ask a doctor before use

  • Inactive ingredients

    Water, Glycerin, PEG-40 Hydrogenated Castor Oil, Chlorhexidine Digluconate, Benzethonium Chloride, Fragrance (Parfum).

  • PRINCIPAL DISPLAY PANEL

    76860-006-01

  • INGREDIENTS AND APPEARANCE
    LITTLE ME SANITIZER 
    little me sanitizer spray spray
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:76860-006
    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
    CHLORHEXIDINE GLUCONATE (UNII: MOR84MUD8E)  
    POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    BENZETHONIUM CHLORIDE (UNII: PH41D05744)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:76860-006-01100 mL in 1 BOTTLE; Type 0: Not a Combination Product04/17/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00304/17/2024
    Labeler - Taizhou Huangyan Liweir Cosmetic Technology Ltd. (560781517)
    Establishment
    NameAddressID/FEIBusiness Operations
    Taizhou Huangyan Liweir Cosmetic Technology Ltd560781517manufacture(76860-006)
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