Label: SOLGREAT ALCOHOL-FREE FOAMING HAND SANITIZER- benzalkonium chloride spray

  • 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 March 27, 2020

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  • Active lngredient  

    Benzalkonium Chloride

  • Purpose 

    Antibacterial

  • Uses

    • hand sanitizer to help reduce bacteria on the skin that could cause disease.
    • recommended for repeated use.

  • Warnings  

    For external use only.

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

    Stop use and ask a doctor if redness or irritation develop and persist for more than 72 hours.

  • Directions

    • place enough product in your palm to thoroughly cover your hands.
    • rub hands together until dry.
    • children under 6 years of age should be supervised when using this product.
  • Inactive Ingredients

    cetrimonium chloride citric acid, cocamidopropyl betaine, cocamidopropylamine oxide, glycerin, propylene glycol, tocopheryl acetate, water.

  • Keep out of reach of children.


    Children must be supervised in use of this product.

  • Other information

    To prevent discoloration, avoid contact with clothing.

  • Product Label - 60 mL SolGreat Alcohol-Free Hand Sanitizer Spray

    60mL

  • Product  Label- 354mL SolGreat Alcohol-Free Foaming Hand Sanitizer

    354ml

  • INGREDIENTS AND APPEARANCE
    SOLGREAT ALCOHOL-FREE FOAMING HAND SANITIZER 
    benzalkonium chloride spray
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:73913-002
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE1.3 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    CETRIMONIUM CHLORIDE (UNII: UC9PE95IBP)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)  
    COCAMIDOPROPYLAMINE OXIDE (UNII: M4SL82J7HK)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:73913-002-0160 mL in 1 BOTTLE; Type 0: Not a Combination Product03/28/2020
    2NDC:73913-002-02354 mL in 1 BOTTLE; Type 0: Not a Combination Product03/28/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A03/28/2020
    Labeler - PANATURAL USA, INC. (029572239)
    Establishment
    NameAddressID/FEIBusiness Operations
    Hefei Yatai Daily-Use Chemical Industry Co., Ltd654641724manufacture(73913-002)
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