Label: BENZALKONIUM CHLORIDE liquid

  • 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 24, 2021

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  • Warning

    Warning: 1. Keep away from heat and flame 2. For children under 6, use only under adult supervision. 3. Keep out of eyes when using this product. 4. Avoid contacting with broken skin.

  • Inactive

    Water, Propylene Glycol, Glycerin, Methylisothiazolinone, Disodium EDTA.

  • Use

    Spray & Sit

  • Active Ingredient:

    Benzethonium Chloride (0.1%)

  • Directions:

    Spray on toilet seat and sit

  • Uses:

    Spray and sit

  • Keep out of reach of children

    Keep out of reach of children

  • Purpose:

    Kills bacteria on toilet seats

  • Toilet Seat Spray

    LabelKills 99.99% of germs

    Spray and sit

    Use anywhere without water

    Recommended for repeated use

    Ingredients Water, Propylene Glycol, Glycerin, Methylisothiazolinone, Disodium EDTA. Active Ingredient Benzalkonium Chloride (0.095%) Directions for use: Spray to toilet seat and enjoy your toilet time. Warning: 1. Keep away from heat and flame 2. For children under 6, use only under adult supervision. 3. Keep out of eyes when using this product. 4. Avoid contacting with broken skin.

  • INGREDIENTS AND APPEARANCE
    BENZALKONIUM CHLORIDE 
    benzalkonium chloride liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:72920-2023
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE30 mg  in 30 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:72920-2023-130 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product11/11/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333E11/11/2019
    Labeler - Plane It Safe LLC (106037472)
    Registrant - Plane It Safe LLC (106037472)
    Establishment
    NameAddressID/FEIBusiness Operations
    Plane It Safe LLC106037472manufacture(72920-2023)
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