Label: BONBLISSITY HAND SANITIZING WIPES- benzalkonium chloride 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 February 23, 2023

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  • Active ingredient

    Benzalkonium Chloride 0.1%

  • Purpose

    Antimicrobial

  • Use

    • Hand sanitizer to help reduce bacteria
  • Warnings

    For external use only

    When using this product do not use in or near the eyes. If contact, rinse eyes thoroughly with water.

    Stop use and ask a doctor if irritation develops and persists 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

    For use apply thoroughly to hands as desired. Allow to dry without wiping. Discard wipe in trash receptacle after use. Do not flush.

    For dispensing peel back front label at tab. Remove towelettes as needed. Reseal pouch by pressing label firmly back into place.

  • Inactive ingredients

    Water, Phenoxyenthanol, Glycerin, Sodium Benzoate, Polysorbate 20, Disodium EDTA, Citric Acid, Tocopheryl Acetate, Aloe Barbadensis Leaf Extract, Fragrance

  • PRINCIPAL DISPLAY PANEL

    Product Label

  • INGREDIENTS AND APPEARANCE
    BONBLISSITY HAND SANITIZING WIPES 
    benzalkonium chloride cloth
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:73582-0002
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE0.01 g  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    SODIUM BENZOATE (UNII: OJ245FE5EU)  
    POLYSORBATE 20 (UNII: 7T1F30V5YH)  
    EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:73582-0002-158 g in 1 POUCH; Type 0: Not a Combination Product06/02/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333E06/02/2020
    Labeler - BONBLISS BEAUTY, INC. (055735749)
    Registrant - BONBLISS BEAUTY, INC. (055735749)
    Establishment
    NameAddressID/FEIBusiness Operations
    FIRSTCHAM CO., LTD694707327manufacture(73582-0002)
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