Label: LIVE LOVE TRAVEL HAND SANITIZER- ethyl alcohol liquid

  • 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 September 30, 2020

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  • Drug Facts

  • Active Ingredient

    Ethyl alcohol 65%

  • Purpose

    Antiseptic

  • INDICATIONS & USAGE

    Uses • to decrease bacteria on the skin that could cause disease • recommended for repeated use

  • Warnings

    For external use only: hands

    Caution • Flammable, keep away from fire or flame.

    When using this product • keep out of eyes. In case of contact with eyes, flush thoroughly with water • avoid contact with broken skin • do not inhale or ingest

    Stop use and ask a doctor if • irritation and redness develop • condition persists for more than 72 hours

    Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

  • DOSAGE & ADMINISTRATION

    Directions • wet hands thoroughly with product and allow to dry without wiping • for children under 6 use only under supervision • not recommended for infants

  • STORAGE AND HANDLING

    Other information • do not store above 105F • may discolor some fabrics • harmful to wood finishes and plastics

  • INACTIVE INGREDIENT

    Inactive ingredients deionized water, aloe vera gel (aloe barbadensis leaf juice), fragrance

  • SPL UNCLASSIFIED SECTION

    fresh scent

    KILLS 99.99% OF GERMS

    *Effective at eliminating more than 99.99% of many common harmful germs and bacteria in as little as 15 seconds.

    Distributed by Fantasy Fragrances, LLC
    Miami, FL 33122

    MADE IN USA

    www.welivelovetravel.com

  • Packaging

    IMAGE

  • INGREDIENTS AND APPEARANCE
    LIVE LOVE TRAVEL HAND SANITIZER 
    ethyl alcohol liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:80523-650
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL65 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:80523-650-0259 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product06/01/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A06/01/2020
    Labeler - Fantasy Fragrances Llc (029592183)
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