Label: AEVI WHENEVER WHEREVER HAND SANITIZER- 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 March 1, 2021

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  • Active Ingredient

    Ethyl Alcohol 70%

  • Purpose

    Antimicrobial

  • Uses:

    Helps to reduce bacteria on the skin. For repeat use.

  • Warnings

    For external use only. Flammable, keep away from heat and flame. Do not store above 104ºF/40ºC.

  • WHEN USING

    When using this product

    • Keep out of eyes. In case of contact with eyes, flush thoroughly with water.

    • Avoid contact with broken skin.

  • STOP USE

    Stop use and ask a doctor if skin irritation develops.

  • KEEP OUT OF REACH OF CHILDREN

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

  • Directions:

    Apply all over your hands and allow to dry. Do not rinse off. For children under 6, use only under adult supervision. Not recommended for infants.

  • Inactive Ingredients

    Aqua (Water), Glycerin, Aloe Barbadensis (Aloe Vera) Leaf Juice*, Pinus Sylvestris Leaf (Nordic Pine) Oil, Eucalyptus Globulus Leaf Oil*, Rosmarinus Officinalis (Rosemary) Oil, Linalool, Limonene.

  • PRINCIPAL DISPLAY PANEL

    Aevi Wellness, Inc
    251 Little Falls Drive
    Wilmington, DE 19808
    Made in USA

    IMGAVHS2OZ

  • INGREDIENTS AND APPEARANCE
    AEVI WHENEVER WHEREVER HAND SANITIZER 
    ethyl alcohol spray
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:62742-4203
    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
    GLYCERIN (UNII: PDC6A3C0OX)  
    EUCALYPTUS OIL (UNII: 2R04ONI662)  
    PINE NEEDLE OIL (PINUS SYLVESTRIS) (UNII: 5EXL5H740Y)  
    ROSMARINUS OFFICINALIS FLOWERING TOP OIL (UNII: OXN0D3N28L)  
    LIMONENE, (+)- (UNII: GFD7C86Q1W)  
    WATER (UNII: 059QF0KO0R)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    LINALOOL, (+/-)- (UNII: D81QY6I88E)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:62742-4203-159 mL in 1 BOTTLE; Type 0: Not a Combination Product02/18/2021
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A02/18/2021
    Labeler - Allure Labs Inc (926831603)
    Registrant - Allure Labs Inc (926831603)
    Establishment
    NameAddressID/FEIBusiness Operations
    Allure Labs Inc926831603manufacture(62742-4203)
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