Label: HAND SANITIZER LUSH ALOE- alcohol spray

  • NDC Code(s): 76891-139-11
  • Packager: SCENT THEORY PRODUCTS LLC
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated October 17, 2024

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  • ACTIVE INGREDIENT

    ETHYL ALCOHOL 62% V/V

  • PURPOSE

    ANTISEPTIC

  • USES

    FOR HANDWASHING TO DECREASE BACTERIA ON THE SKIN.

  • WARNINGS

    FOR EXTERNAL USE ONLY: HANDS

    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

    Keep out of reach of children.

    If swallowed, get medical help or contact a Poison Control Center right away.

  • DIRECTIONS

    • SPRAY HANDS WITH PRODUCT AND ALLOW TO DRY WITHOUT WIPING
    • FOR CHILDREN UNDER 6, USE ONLY UNDER ADULT SUPERVISION
    • NOT RECOMMENDED FOR INFANTS
  • OTHER INFORMATION

    • DO NOT STORE ABOVE 105°F
    • MAY DISCOLOR SOME FABRICS
    • HARMFUL TO WOOD FINISHES AND PLASTICS
  • INACTIVE INGREDIENTS

    WATER, ALOE BARBADENSIS LEAF JUICE, GLYCERIN, FRAGRANCE, EUCALYPTUS GLOBULUS LEAF OIL, DENATONIUM BENZOATE

  • PRINCIPAL DISPLAY PANEL

    LBL

  • INGREDIENTS AND APPEARANCE
    HAND SANITIZER  LUSH ALOE
    alcohol spray
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:76891-139
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL62 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    DENATONIUM BENZOATE (UNII: 4YK5Z54AT2)  
    EUCALYPTUS GLOBULUS LEAF (UNII: S546YLW6E6)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:76891-139-1130 mL in 1 BOTTLE; Type 0: Not a Combination Product10/15/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00310/15/2024
    Labeler - SCENT THEORY PRODUCTS LLC (101216246)
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