Label: BOOGIE HANDS ANTIBACTERIAL WET WIPES (benzalkonium chloride- 0.115% cloth

  • NDC Code(s): 79747-007-02, 79747-007-20, 79747-007-30
  • Packager: ELEEO BRANDS LLC
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated March 2, 2024

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  • Active ingredients

    Benalkonium chloride (0.115%)

  • Purpose

    Antibacterial

  • Use

    For hand sanitizing to decrease bacteria on skin

  • Warnings

    For external use only

  • Do Not Use

    if you are allergic to any of the ingredients

  • When using this product

    donot get into eyes.

    if contact occurs, rinse thoroughly with water.

  • Stop use and ask a doctor if

    irritation or rash develops.

    and continues for more than 72 hours

  • 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 to dry without wiping

    *children under 2 years

    • ask a doctor before use 
  • Inactive ingredients

    Water, Gycerin, Fragrance, Aloe extract, Disodium EDTA , Propylene Glycol, Sorbitol

  • PRINCIPAL DISPLAY PANEL

    1

  • PRINCIPAL DISPLAY PANEL

    bbsamaa

  • INGREDIENTS AND APPEARANCE
    BOOGIE HANDS ANTIBACTERIAL WET WIPES 
    benzalkonium chloride (0.115%) cloth
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:79747-007
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE0.0012 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    SORBITOL (UNII: 506T60A25R)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    EDETATE SODIUM (UNII: MP1J8420LU)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:79747-007-203 in 1 CARTON07/22/2020
    120 mL in 1 POUCH; Type 0: Not a Combination Product
    2NDC:79747-007-0220 mL in 1 PACKET; Type 0: Not a Combination Product07/22/2020
    3NDC:79747-007-301 in 1 CARTON07/22/2020
    330 mL in 1 PACKET; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)07/22/2020
    Labeler - ELEEO BRANDS LLC (078476782)
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