Label: ZEST HAND SANITIZER- ethyl alcohol gel

  • 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 15, 2020

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  • ACTIVE INGREDIENT

    ETHYL ALCOHOL (70% w/v)

  • PURPOSE

    ANTIMICROBIAL

  • USES

    HAND SANITIZER TO HELP REDUCE BACTERIA THAT CAN POTENTIALLY CAUSE DISEASE. FOR USE WHEN SOAP AND WATER ARE NOT AVAILABLE.

  • WARNINGS

    • FLAMMABLE.
    • KEEP AWAY FROM FIRE OR FLAME.
    • FOR EXTERNAL USE ONLY.

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

    Stop use and ask a doctor if irritation or rash appears and lasts.

  • 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

    • Put enough product in your palm to cover hands and rub hands together briskly until dry.
    • Children under 6 years of age should be supervised when using this product.

  • OTHER INFORMATION

    • Store below 110°F (43°C)
    • May discolor certain fabrics.

  • INACTIVE INGREDIENTS

    WATER, PEG-8, PROPYLENE GLYCOL, ACRYLATES/C10-30 ALKYL ACRYLATE CROSSPOLYMER, TERT-BUTYL ALCOHOL, AMINOMETHYL PROPANOL, TOCOPHERYL ACETATE, DENATONIUM BENZOATE.

  • PRINCIPAL DISPLAY PANEL

    01b LBL_Zest Hand Sani Gel_70pct EtOH_8oz

  • INGREDIENTS AND APPEARANCE
    ZEST HAND SANITIZER 
    ethyl alcohol gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:81277-102(NDC:77352-102)
    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
    WATER (UNII: 059QF0KO0R)  
    POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)  
    AMINOMETHYLPROPANOL (UNII: LU49E6626Q)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    AGASTACHE FOENICULUM WHOLE (UNII: ZV7TA06J2V)  
    AGAVE TEQUILANA LEAF (UNII: 05545M0E3M)  
    LEMON PEEL (UNII: 72O054U628)  
    COFFEE BEAN (UNII: JFH385Y744)  
    MALPIGHIA GLABRA FRUIT (UNII: B94O42LA9M)  
    GLYCOLIC ACID (UNII: 0WT12SX38S)  
    ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
    MALIC ACID (UNII: 817L1N4CKP)  
    FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
    FD&C YELLOW NO. 6 (UNII: H77VEI93A8)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:81277-102-08236 mL in 1 BOTTLE; Type 0: Not a Combination Product12/15/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A12/15/2020
    Labeler - TCP HRB HOLDINGS LLC (117465959)
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