Label: MY INSTANT HAND SANITIZER WITH ALOE AND VITAMIN E- 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 July 3, 2013

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  • MY INSTANT HAND SANITIZER with aloe & vitamin e


  • Active ingredient

    Ethyl Alcohol 62%

  • Purpose

    Antiseptic

  • Uses

    • A hand sanitizer to help reduce bacteria on the skin
  • Warnings

    For external use only

    Flammable.

    Keep away from fire or flame or sparks

    When using this product

    do not use in or near eyes. In case of contact, rinse eyes thoroughly with water.

    Stop use and ask a doctor if

    irritation or rash appears on the skin

    Keep out of reach of children.

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

  • Directions

    • Place enough to cover both hands in the palm, and rub hands together until dry.
    • Children under 6 years of age should be supervised by adult when applying this product
  • Other information

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

  • Inactive ingredient

    Purified water triethanolamine, glycerin, propylene glycol, tocopheryl acetate, carbomer, aloe barbadensis leaf juice, fragrance.

  • DISTRIBUTED BY:

    MAPCO EXPRESS, INC.,
    7102 COMMERCE WAY, BRENTWOOD, TN 37027
    Made in China

    MY 100% Satisfaction Guarantee:
    If you don’t love it we will refund or replace it!

    0  24291 27672  2

  • PRINCIPAL DISPLAY PANEL

    MY kills 99.99% of germs

    INSTANT HAND SANITIZER with aloe and vitamin e

    2 FL OZ. (59mL)

  • MY INSTANT HAND SANITIZER with aloe & vitamin e 2oz/59ml (59086-085-07)

    Hand Sanitizer

  • INGREDIENTS AND APPEARANCE
    MY INSTANT HAND SANITIZER WITH ALOE AND VITAMIN E  
    ethyl alcohol gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:59086-085
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL620 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:59086-085-071 in 1 CARTON
    159 mL in 1 BOTTLE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333E07/03/2013
    Labeler - Mapco Express (024941077)
    Establishment
    NameAddressID/FEIBusiness Operations
    Ningbo Pulisi Daily Chemical Products Co.,Ltd.529047265manufacture(59086-085)
    Establishment
    NameAddressID/FEIBusiness Operations
    Navajo Manufacturing Company Inc091917799relabel(59086-085) , repack(59086-085)
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