Label: HAND SANITIZER FRESH EVERGREEN- isopropyl alcohol 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 August 25, 2020

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  • Active Ingredient

    Isopropyl alcohol 70% v/v

  • Purpose

    Antiseptic

  • Use

    To help reduce bacteria on the skin.

  • Warnings

    • For external use only.
    • Flammability warning. Keep away from heat or flame.

    Do not useon children less than 2 years of age (unless directed by a doctor).

    When using this product avoid contact with eyes. If contact occurs, rinse thoroughly with water.

    Stop use and consult a doctor if irritation develops.

  • KEEP OUT OF REACH OF CHILDREN

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

  • Directions

    • Dispense enough product in your palm to thoroughly cover your hands.
    • Rub hands together briskly until dry.
  • Inactive ingredients

     Aloe Vera Extract, Bergamot Essential Oil, Fir Needle Essential Oil, Fragrance, Water.

    Questions?

    Contact Scentuals at +1877-770-7590 Mon-Fri 9am - 4pm PST.

  • Package Label - Principal Display Panel

    Label

  • INGREDIENTS AND APPEARANCE
    HAND SANITIZER FRESH EVERGREEN 
    isopropyl alcohol spray
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:79883-009
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302) ISOPROPYL ALCOHOL70 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    BERGAMOT OIL (UNII: 39W1PKE3JI)  
    ABIES SIBIRICA LEAF OIL (UNII: XRY0V4VZKZ)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:79883-009-0160 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product07/01/2020
    2NDC:79883-009-02120 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product07/01/2020
    3NDC:79883-009-03250 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product07/01/2020
    4NDC:79883-009-04500 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product07/01/2020
    5NDC:79883-009-051000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product07/01/2020
    6NDC:79883-009-063785 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product07/01/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A07/01/2020
    Labeler - TAICORP ENTERPRISES LIMITED (202875738)
    Establishment
    NameAddressID/FEIBusiness Operations
    TAICORP ENTERPRISES LIMITED202875738manufacture(79883-009)
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