Label: ELIVE HAND SANITIZER- 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 7, 2020

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  • Drug Facts

  • Active ingredient

    Ethyl alcohol 72%

    Purpose

    Antiseptic

  • Use

    for hand washing to decrease bacteria on the skin

  • Warnings

    For external use only
    Flammable, keep away from fire or flame.

    Do not use

    in the eyes

    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.

  • Directions

    wet hands thoroughly with product and allow to dry without wiping

  • Inactive ingredients

    water, glycerin, jojoba oil PEG-150 esters, tocopherol, aloe vera extract, panthenol, Japanese honeysuckle flower extract, wild chrysanthemum flower extract, Sophora ( Sophora angustifolia) root extract, peppermint leaf extract, Chinese skullcap root extract, acylates/C10-30 alkyl acrylate crosspolymer, triethanolamine.

  • Package Labeling:240ml

    240ml Label240ml Label2

  • Package Labeling:500ml

    500ml Label500ml Label2.jpg

  • INGREDIENTS AND APPEARANCE
    ELIVE HAND SANITIZER 
    alcohol gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:79123-000
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL0.72 mL  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    JOJOBA OIL (UNII: 724GKU717M)  
    TOCOPHEROL (UNII: R0ZB2556P8)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    PANTHENOL (UNII: WV9CM0O67Z)  
    SOPHORA FLAVESCENS ROOT (UNII: IYR6K8KQ5K)  
    CHRYSANTHEMUM INDICUM FLOWER (UNII: I6OER6U04L)  
    MENTHA PIPERITA LEAF (UNII: A389O33LX6)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:79123-000-01240 mL in 1 BOTTLE; Type 0: Not a Combination Product07/02/2020
    2NDC:79123-000-02500 mL in 1 BOTTLE; Type 0: Not a Combination Product07/02/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333E07/02/2020
    Labeler - Provendex Pty Ltd (742436587)
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