Label: NANO MINI VANILLA HAND SANITIZER- ethyl alcohol liquid

  • 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 18, 2020

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  • Active Ingredient

    Ethyl Alcohol    70%

  • Purpose

    Antiseptic.

  • Use [s]

    • for handwashing to decrease bacteria on the skin that could cause disease.
    • recommended for repeated use.
  • Warnings

    For external use only
    Flammable, keep away from fire or flame

    Do not use • in or near the eyes

    When using this product keep out of eyes, ears, and mouth.

    • In case of contact with eyes, rinse eyes thoroughly with water rinse eyes thoroughly with water

    Stop use and ask a doctor if

    • irritation and redness develop.
    • condition persists for more than 72 hours.

  • Keep out of reach of children.

    If swallowed, get medical help or contact a Poison Control Center right away.

  • Directions

    • wet hands thoroughly with product and to dry without wiping

    • children under 6 years of ages should be supervised when using this product.

    • Not recommended for infants.

  • Other information

    • Avoid freezing and excessive heat above 104º F (40º C).
    • Store between 15-30º C (59-86 ºF)
    • When exposed to light, liquid solution color may very without effecting the effectiveness of formula.
  • Inactive ingredients

    Aloe Vera, Fragrance (parfum), Glycerin, Grape Seed Oil, Isopropyl Myristate, Propylene glycol, Water, FD&C Yellow #5.

  • PRODUCT IMAGE

    image description

  • INGREDIENTS AND APPEARANCE
    NANO MINI VANILLA HAND SANITIZER 
    ethyl alcohol liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:81231-011
    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
    ALOE VERA WHOLE (UNII: KIZ4X2EHYX)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    GRAPE SEED OIL (UNII: 930MLC8XGG)  
    ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    WATER (UNII: 059QF0KO0R)  
    FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:81231-011-0145 mL in 1 CONTAINER; Type 0: Not a Combination Product11/09/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A11/09/2020
    Labeler - DISINFEKT ENVIRONMENTAL SOLUTIONS FZE (851677306)
    Establishment
    NameAddressID/FEIBusiness Operations
    DISINFEKT ENVIRONMENTAL SOLUTIONS FZE851677306manufacture(81231-011)
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