Label: HEALING POOLS MOISTURIZING ALOE ANTIBACTERIAL WET WIPE- benzalkonium chloride solution

  • 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 November 2, 2021

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  • Active Ingredient

    Benzalkonium Chloride 0.1%

  • Purpose

    Antimicrobial

  • Use

    Antibacterial wipe to help reduce bacteria

  • Warnings

    Non Medical. For external use only.

    Keep away from heat or flame

    Avoid contact with eyes. If contact occurs, flush eyes with water

  • STOP USE

    Stop use and consult a doctor if irritation or rash occurs. 

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children. If swallowed, seek immediate medical help or contact a poison control center

  • Directions

    • Apply to intended area as needed. Discard after single use
  • Other Information

    Store below 110F (43C)

  • Inactive ingredients

    Water, Glycerin, Phenoxyethanol, Didecyldimonium Chloride, Ethylhexylglycerin, Propylene Glycol, Aloe Vera Extract

  • PRINCIPAL DISPLAY PANEL

    image description

  • INGREDIENTS AND APPEARANCE
    HEALING POOLS MOISTURIZING ALOE ANTIBACTERIAL WET WIPE 
    benzalkonium chloride solution
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:73027-214
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE1.7 mg
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX)  
    ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
    WATER (UNII: 059QF0KO0R)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    DIDECYLDIMONIUM CHLORIDE (UNII: JXN40O9Y9B)  
    ALOE VERA WHOLE (UNII: KIZ4X2EHYX)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:73027-214-011 in 1 POUCH; Type 0: Not a Combination Product09/11/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A09/11/2020
    Labeler - JIANGSU HANHE DAILY CHEMICALS CO., LTD. (414409758)
    Establishment
    NameAddressID/FEIBusiness Operations
    JIANGSU HANHE DAILY CHEMICALS CO., LTD.414409758manufacture(73027-214)
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