Label: ASSURED INSTANT HAND SANITIZER WITH MOISTURIZERS VITAMIN E AND ALOE- 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 April 17, 2019

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  • WARNINGS AND PRECAUTIONS

    Assured Instant Hand Sanitizer with Moisturizers Vitamin E and Aloe

  • Active Ingredient

    Ethyl Alcohol 62.0%

  • Purpose

    Antimicrobial

  • Uses

    • for handwashing to decrease bacteria on the skin
    • recommended for repeated use
  • Warnings

    For external use only.

  • SAFE HANDLING WARNING

    Flammable, keep away from heat and flame.

  • Do not use

    in the eyes.  In case of contact, rinse eyes thorougly with water.

  • Stop use and ask a doctor if

    irritation and redness develop and persist 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
    • briskly rub hands together until dry
    • supervise children under 6 years in the use of this product
  • Other Information

    • store at 20 degrees C (68 to 77 degrees F).
    • may discolor certain fabrics.
  • Inactive Ingredients

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

  • DESCRIPTION

    This product is not manufactured by Gojo Industries, Inc, distributor of the registered trademark Purell.

    Distributed By: GREENBRIER INTERNATIONAL, INC.,

    CHESAPEAKE, VA 23320

    MADE IN CHINA

  • PRINCIPAL DISPLAY PANEL

    label image

    outer package image

  • INGREDIENTS AND APPEARANCE
    ASSURED INSTANT HAND SANITIZER WITH MOISTURIZERS VITAMIN E AND ALOE 
    alcohol gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:33992-1071
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL62 mL  in 100 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:33992-1071-42 in 1 PACKAGE05/10/2012
    1NDC:33992-1071-059.2 mL in 1 BOTTLE; Type 0: Not a Combination Product
    2NDC:33992-1071-3295 mL in 1 BOTTLE; Type 0: Not a Combination Product05/10/2012
    3NDC:33992-1071-5237 mL in 1 BOTTLE; Type 0: Not a Combination Product05/10/2012
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333E05/10/2012
    Labeler - Greenbrier International, Inc. (610322518)
    Establishment
    NameAddressID/FEIBusiness Operations
    Ningbo Pulisi Daily Chemical Products Co.,Ltd.529047265manufacture(33992-1071)
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