Label: LUCKY SANITIZING HAND TOWELS- alcohol cloth

  • 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 August 8, 2013

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  • Active Ingredient

    Ethyl alcohol 62%

  • Purpose

    Antiseptic

  • Uses

    Sanitizing Hand Towel to help bacteria on the skin. Recommended for repeated use

  • WARNINGS

    Flammable. Keep away from fire or flame.

    For external use only

  • When using this product


    avoid contact with eyes. In case of eye contact immediately flush eyes with water, call a doctor.
    Avoid contact with broken skin.

  • Discontinue use

    if irritation or redness develops. If condition persists for more than 72 hours, consult a doctor

  • Keep out of reach of children

    Children can only use this product with adult supervision. Do not drink. Not edible, in case of accidental ingestion seek professional assistance or contact a Poison Control Center immediately

  • Directions

    Open the foil packet, unfold towel and wipe your hands. After use dispose properly. Do not flush down toilet

  • INACTIVE INGREDIENTS

    Water, Isopropyl Alcohol, Isopropyl Myristate, Propylene Glycol, Sodium Polyacrylate, Hydrogenated Polydecene, Trideceth-6, Fragrance, Glycerin, Polyquaternium-7, Tocopheryl Acetate, Methylchloroisothiazolinine, Methylisothiazolinone,  Aloe Barbadensis Leaf Extract (Aloe Vera), Fragrance, Corn Oil

  • Package Label

    image description

  • INGREDIENTS AND APPEARANCE
    LUCKY  SANITIZING HAND TOWELS
    alcohol cloth
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:20276-430
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL62 mg
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    ISOPROPYL ALCOHOL (UNII: ND2M416302)  
    ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    SODIUM POLYACRYLATE (8000 MW) (UNII: 285CYO341L)  
    HYDROGENATED POLYDECENE (550 MW) (UNII: U333RI6EB7)  
    TRIDECETH-6 (UNII: 3T5PCR2H0C)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)  
    METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    CORN OIL (UNII: 8470G57WFM)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:20276-430-1010 in 1 BOX
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A07/01/2013
    Labeler - Delta Brands, Inc (102672008)
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