Label: CHERRY BLOSSOM SCENTED ANTISEPTIC HAND SANITIZER 80 ETHYL ALCOHOL- alcohol liquid

  • NDC Code(s): 82127-000-01, 82127-000-02
  • Packager: H&Y Products LLC dba Kolonya Carre
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 29, 2023

If you are a consumer or patient please visit this version.

  • Drug Facts

  • Active ingredient

    Ethyl alcohol 80%

    Purpose

    Antiseptic

  • Use

    for hand washing to decrease bacteria on the skin.

  • Warnings

    For external use onlyFlammable, 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, Fragrance, Alpha isomethyl ionone, Butylphenyl methylpropional, Citronellol, Coumarin, Isoeugenol, Linalool

  • Package Labeling:82127-000-01

    Outer PackageInner Package

  • Package Labeling:82127-000-02

    Outer Package.2Inner Package2

  • INGREDIENTS AND APPEARANCE
    CHERRY BLOSSOM SCENTED ANTISEPTIC HAND SANITIZER 80 ETHYL ALCOHOL 
    alcohol liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:82127-000
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL80 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    ISOMETHYL-.ALPHA.-IONONE (UNII: 9XP4LC555B)  
    BUTYLPHENYL METHYLPROPIONAL (UNII: T7540GJV69)  
    .BETA.-CITRONELLOL, (R)- (UNII: P01OUT964K)  
    COUMARIN (UNII: A4VZ22K1WT)  
    ISOEUGENOL (UNII: 5M0MWY797U)  
    LINALOOL, (+/-)- (UNII: D81QY6I88E)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:82127-000-011 in 1 BOX08/01/202107/31/2025
    135 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
    2NDC:82127-000-021 in 1 BOX08/01/202107/31/2025
    290 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)08/01/202107/31/2025
    Labeler - H&Y Products LLC dba Kolonya Carre (070644433)