Label: SMART CARE HAND SANITIZER PISTACHIO BRULEE- ethyl alcohol spray

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated April 17, 2025

If you are a consumer or patient please visit this version.

  • Drug Facts

  • Active ingredient

    Ethyl Alcohol 70% v/v

  • Purpose

    Antiseptic

  • Uses

    Decreases bacteria on skin.

  • Warnings

    For external use only

    Flammable, keep away from fire or flame.

    Do not use • If you are allergic to any of the ingredients.

    When using this product • Do not get into eyes. If contact occurs, rinse thoroughly with water.

    Stop use and ask a doctor • If irritation or rash develops and continues for more than 72 hours.

    Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center immediately.

  • Directions

    Adults and children 6 years and older
      Spray onto hands and rub them together until dry. Recommended for repeated use.

    Children under 6 years of age
      Should be supervised when using this product.

  • Other information

    • Store between 15-30°C (59-86°F)
    • Avoid freezing and excessive heat above 40°C (104°F)

  • Inactive ingredients

    Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Aloe Barbadensis Gel, Aminomethyl Propanol, Blue 1, Denatonium Benzoate, Fragrance, Glycerin, PEG-40 Hydrogenated Castor Oil, Tocopheryl Acetate, Water, Yellow 5

  • Questions or comments?

    Call toll free 1-877-274-8358

  • SPL UNCLASSIFIED SECTION

    *Effective at killing 99.9% of Escherichia coli, Staphylococcus aureus under laboratory settings

    Smart Care® SMARTCAREUS.COM
    1-909-434-0911 INTERNATIONAL

    COPYRIGHTS AND TRADEMARKS GRANTED OR PENDING WORLDWIDE

    DISTRIBUTED BY ASHTEL STUDIOS INC.
    ONTARIO, CALIFORNIA 91761

  • Packaging

    PISTACHIOBRULEESANITIZER-1

  • INGREDIENTS AND APPEARANCE
    SMART CARE HAND SANITIZER PISTACHIO BRULEE 
    ethyl alcohol spray
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:70108-147
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL70 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    ACRYLATES/C10-30 ALKYL ACRYLATE CROSSPOLYMER (60000 MPA.S) (UNII: 8Z5ZAL5H3V)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    AMINOMETHYLPROPANOL (UNII: LU49E6626Q)  
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    DENATONIUM BENZOATE (UNII: 4YK5Z54AT2)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    WATER (UNII: 059QF0KO0R)  
    FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:70108-147-0130 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product05/15/2025
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)05/15/2025
    Labeler - Ashtel Studios, Inc. (148689180)