Label: LIFE IS SIMPLE HAND SANITIZER- non-alcohol foaming hand sanitizer aerosol, foam

  • NDC Code(s): 63148-500-10
  • Packager: Apollo Health and Beauty Care Inc
  • 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 14, 2020

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  • Active Ingredients

    Benzalkonium Chloride 0.1%

  • Purpose

    Antiseptic

  • Uses

    To help decrease bacteria on the skin. For use when soap and water are not available.

  • Warnings

    For External use only

    When using this product

    Avoid contact with eyes. If contact occurs, rinse thoroughly with water.

    Do not use

    • on children less than 2 months of age.
    • on open wounds. 

    Stop use and ask a doctor

    If irritation or redness develops and lasts more than 7 days.

    Keep out of reach of children

    In case of accidental ingestion, get medical help or contact a Poison Control Centre immedoately

  • Directions

    • Pump enough product to your palm to thoroughly cover your hands, rub together for at least 30 seconds, until dry.
    • Children under 6 years should be supervised when using this product.

  • Other information

    • Store at room temperature

  • Inactive Ingredients

    Water, Polysorbate 20, PPG-26-Buteth-26, PEG-40 Hydrogenated Castor Oil, Aloe Barbadensis Leaf Juice, Fragrance (Parfum), Camellia Sinensis Leaf Extract, DMDM Hydantoin, Sodium Hydroxide, Blue 1 (CI 42090), Yellow 5 (CI 19140)

  • Questions or comments ?

    1-866-695-3030

  • Package Label

    Life is simple Hand Sanitizer

  • INGREDIENTS AND APPEARANCE
    LIFE IS SIMPLE HAND SANITIZER 
    non-alcohol foaming hand sanitizer aerosol, foam
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:63148-500
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE1.0 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    POLYSORBATE 20 (UNII: 7T1F30V5YH)  
    PPG-26-BUTETH-26 (UNII: 2II1K6TZ4P)  
    POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    GREEN TEA LEAF (UNII: W2ZU1RY8B0)  
    DMDM HYDANTOIN (UNII: BYR0546TOW)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:63148-500-10296 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product12/10/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333E10/06/2020
    Labeler - Apollo Health and Beauty Care Inc (201901209)
    Registrant - Apollo Health and Beauty Care Inc (201901209)
    Establishment
    NameAddressID/FEIBusiness Operations
    Apollo Health and Beauty Care Inc201901209manufacture(63148-500)
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