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

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph not final

DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Drug Label Information

Updated December 7, 2022

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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

    2

  • INGREDIENTS AND APPEARANCE
    BOOGIE HANDS ANTIBACTERIAL WET WIPES 
    benzalkonium chloride (0.115%) cloth
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:79747-005
    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:79747-005-203 in 1 CARTON07/22/2020
    120 mL in 1 POUCH; Type 0: Not a Combination Product
    2NDC:79747-005-0220 mL in 1 PACKAGE; Type 0: Not a Combination Product07/22/2020
    3NDC:79747-005-301 in 1 CARTON07/22/2020
    330 mL in 1 POUCH; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A07/22/2020
    Labeler - ELEEO BRANDS LLC (078476782)
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