Label: INSTANT HAND SANITIZER- alcohol liquid

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph 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 25, 2012

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  • Drug Facts


  • Active Ingredient:

    Ethyl Alcohol 62% w/w

  • Purpose

    Antiseptic

  • Uses:

    For handwashing 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 the eyes. In case of contact, rinse eyes thoroughly 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 in the use of this product.


  • Inactive Ingredients

    Ethanol, Deionized water, Carbomer, Triethanolamine, 2H-1-Benzopyran-6-ol,3,4-dihydro-2,5,7,8-tetramethyl-2-(4,8,12-trimethyltridecyl)-acetate.

  • Other Information

    Do not store above 105 degrees F.

    May discolor some fabrics or surfaces.

    This product is not made by "PFIZER Industries Inc."

    Owner of the registered trademark "Purell"


    All Rights Reserved

    Distributed By:

    LONKEY OVERSEAS INCORPORATION

    MADE IN CHINA

  • Instant Hand Sanitizer 8oz/236ml (42302-030-00)

    with MOISTURIZERS,
    VITAMIN E

    Leaves Hands Feeling
    Soft and Refreshed

    Instant
    Hand Sanitizer

    COMPARE to Purell

    KILLS GERMS
    WITHOUT WATER

    Kills 99.99% of most common germs
    that may cause illness

    Item No 00241

    8 FL. OZ (236 ml)

    InstantHandSanitizer

  • INGREDIENTS AND APPEARANCE
    INSTANT HAND SANITIZER 
    alcohol liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:42302-030
    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
    ALCOHOL (UNII: 3K9958V90M)  
    WATER (UNII: 059QF0KO0R)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    .ALPHA.-TOCOPHEROL ACETATE, D- (UNII: A7E6112E4N)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:42302-030-00236 mL in 1 BOTTLE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart333E01/25/2012
    Labeler - Lonkey Overseas Inc. (017448266)
    Registrant - Lonkey Industrial Co., Ltd. Guangzhou (654539139)
    Establishment
    NameAddressID/FEIBusiness Operations
    Lonkey Industrial Co., Ltd. Guangzhou654539139manufacture
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