Label: HAND SANITIZER 70%- ethyl 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 January 15, 2022

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  • ACTIVE INGREDIENTS

    ETHYL ALCOHOL 70% v/v

  • PURPOSE

    ANTISEPTIC

  • USES

    ■ TO DECREASE BACTERIA ON THE SKIN

    ■ RECOMMENDED FOR REPEATED USE

  • WARNINGS

    For external use only.

    Flammable, Keep away from fire or flame.

    Do not use in or near the eyes • In case of contact, rinse eyes thoroughly with water •Avoid contact with broken skin.

    Stop use and ask a doctor if • irritation or redness develops •condition persists for more than 72 hours.

  • 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

    • place enough product in your palms to thoroughly cover your hands
    • children under the age of 6 years of age should be supervised when using this product
    • rub hands together briskly until dry

    Other Information

    • protect the product in the container from excessive heat and direct sun

    • store below 104°F (40°C) •may discolor certain favrics

  • INACTIVE INGREDIENTS

    ROSEWATER: Water, Propanediol, Aloe Barbadensis Leaf Juice, Leuconostoc/ Radish Root Ferment Lysate Filtrate, Glycereth-26, Baicalin, Glycerin, Citrus Aurantifolia (Lime) Oil, Citrus Limon (Lemon) Peel Oil,Paeonia Lactiflora Root Extract, Trehalose, Fragrance, Linalool, Geraniol, Hexyl Cinnamal, Alpha-lsomethyl lonone, Citronellol, Citral.

  • PRINCIPAL DISPLAY PANEL

    1b LBL_Touchland_Hand Sanitizer Mist_30ML.jpg

  • INGREDIENTS AND APPEARANCE
    HAND SANITIZER  70%
    ethyl alcohol spray
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:72033-407
    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
    PROPANEDIOL (UNII: 5965N8W85T)  
    .ALPHA.-HEXYLCINNAMALDEHYDE (UNII: 7X6O37OK2I)  
    WATER (UNII: 059QF0KO0R)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    LEUCONOSTOC/RADISH ROOT FERMENT FILTRATE (UNII: D2QHA03458)  
    GLYCERETH-26 (UNII: NNE56F2N14)  
    BAICALIN (UNII: 347Q89U4M5)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    LIME OIL, COLD PRESSED (UNII: UZH29XGA8G)  
    LEMON OIL, COLD PRESSED (UNII: I9GRO824LL)  
    TREHALOSE (UNII: B8WCK70T7I)  
    LINALOOL, (+/-)- (UNII: D81QY6I88E)  
    ISOMETHYL-.ALPHA.-IONONE (UNII: 9XP4LC555B)  
    CITRAL (UNII: T7EU0O9VPP)  
    GERANIOL (UNII: L837108USY)  
    .BETA.-CITRONELLOL, (R)- (UNII: P01OUT964K)  
    PAEONIA LACTIFLORA ROOT (UNII: 3Z3866YW6P)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:72033-407-1130 mL in 1 BOTTLE; Type 0: Not a Combination Product11/17/2021
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A11/17/2021
    Labeler - TOUCHLAND LLC (036656461)
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