Label: LE VITAL MOON TO LIGHT- 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 31, 2015

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  • ACTIVE INGREDIENT

    Mecicical Ingredient

    Ethyl Alcohol 62%

    Purpose

    Antiseptic

  • PURPOSE

    Features

    To decrease bacteria on the skin that could cause disease.

    • Recommended for repeated use.
    • Use anywhere without water.
  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children. In case of accidental ingestion, seek professional assistance or contact a Poison Control Center immediately.

  • INDICATIONS & USAGE

    Le Vital ® Signature

    moon to light

    hand sanitizer 

  • DOSAGE & ADMINISTRATION

    Directions

    • Wet hands thoroughly with product and rub until dry without wiping
    • For children under 6, use only under adult supervision.
    • Not recommended for infants
  • WARNINGS

    Warning

    • For external use only - hands
    • Flammable, keep away from heat and flame
    • Discontinue if skin becomes irritated and ask a doctor

    CAUTION: For external use only. This product was not tested on animals.

    When using this product

    • Keep out of eyes. In case of contact with eyes, flush thoroughly with water.
    • Do not inhale or ingest.
    • Avoid contact with broken skin.

    Other information

    • Do not store above 105°F.
    • May discolor some fabrics.
    • Harmful to wood finishes and plastics.
  • INACTIVE INGREDIENT

    Non-Medicinal

    water, isopropyl alcohol, glycerin, carbomer, aminomethyl propanol, parfum, propylene glycol, isopropyl myristate, aloe barbadensis leaf juice, tacopheryl acetate

  • PRINCIPAL DISPLAY PANEL

    image description

  • INGREDIENTS AND APPEARANCE
    LE VITAL MOON TO LIGHT 
    ethyl alcohol gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:50306-007
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL62 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    ISOPROPYL ALCOHOL (UNII: ND2M416302)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    CARBOMER COPOLYMER TYPE A (UNII: 71DD5V995L)  
    AMINOMETHYLPROPANOL (UNII: LU49E6626Q)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:50306-007-0129 g in 1 PACKAGE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333E07/23/2015
    Labeler - Shanghai Lantern Cosmetic Co., Ltd. (421252043)
    Establishment
    NameAddressID/FEIBusiness Operations
    Shanghai Lantern Cosmetic Co., Ltd.421252043manufacture(50306-007)
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