Label: HAND SANITIZER LEMON SCENT HAND RX- ethyl alcohol gel

  • NDC Code(s): 22431-132-01, 22431-132-02
  • Packager: Blue Cross Laboratories, Inc.
  • Category: HUMAN OTC DRUG LABEL

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 27, 2017

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  • ACTIVE INGREDIENT

    Active ingredient              Purpose

    Ethyl Alcohol  62.0%        Antimicrobial

    Uses hand sanitizer to help reduce bacteria on the skin that may cause disease

    keep out of reach. If swallowed, get medical help or contact a Poison Control Center.

    Stop use and ask a doctor if irritation or redness develops

    Warnings

    For external use only

    Flammable. Keep away from heat and flame.

    When using this product avoid contact with face, eyes, and broken skin. In case of eye contact, flush with plenty of water and seek medical advice.

    Directions

    wet hands thoroughly with product and rub into skin until dry

    Children under 6 years of age should be supervised by an adult when using this product.

    Inactive Ingredients water (aqua), triethanolamine, carbomer, aloe barbadensis leaf juice, fragrance, glycerin, propylene glycol, tocopheryl acetate (vitamin E).

  • PRINCIPAL DISPLAY PANEL


    Hand Rx

    Hand Sanitizer

    Kills 99.99% of Germs

    Leaves Hands Feeling Soft

    Lemon Scent

    2 FL OZ (59 mL)

    package

    Bottle

  • INGREDIENTS AND APPEARANCE
    HAND SANITIZER LEMON SCENT  HAND RX
    ethyl alcohol gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:22431-132
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL62 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    CARBOMER HOMOPOLYMER TYPE B (ALLYL SUCROSE CROSSLINKED) (UNII: Z135WT9208)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:22431-132-022 in 1 BLISTER PACK08/19/2014
    1NDC:22431-132-0159 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333E08/19/2014
    Labeler - Blue Cross Laboratories, Inc. (008298879)
    Registrant - Blue Cross Laboratories, Inc. (008298879)
    Establishment
    NameAddressID/FEIBusiness Operations
    Ningbo Liyuan Daily Chemical Products Co., Ltd.530766098manufacture(22431-132)
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