Label: CLEAR HANI-TIZER- 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 March 5, 2020

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  • Active Ingredient

    Ethanol 70%

  • Purpose

    Hand Sanitizer

  • Uses

    An antiseptic hand sanitizer for topical application.

    Helps prevent infection and cross-contamination.

    Reduces transient microorganisms on intact skin.

    Recommended for repeated use.

  • Warnings

    For external use only

    Flammable, keep away from fire or flame.

    When using this product avoid contact with eyes.

    In case of eye contact, flush with water 15 minutes.

    Discontinue use and see a doctor if irritation occurs.

    Avoid contact with broken skin.

    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.

    Allow to dry without wiping.

    Use no water or towels.

  • Inactive ingredients

    Purified Water, Carbomer, Isopropanol, Glycerin, Aloe Barbadensis Leaf Juice, Tocopherol (Vitamin E), Isopropyl Myristate, Diisopropyl Sebacate, Propylene Glycol, Aminomethyl Propanol, Fragrance, Yellow 5, Blue 1.

  • Questions?

    Call 1-855-797-2257

  • PRINCIPAL DISPLAY PANEL

    CLEAR

    The Choice Is Clear

    HANI-TIZER

    Germ Barrier

    purpose:

    germ assassin

    scent:

    fresh

    benefits:

    easy to use

    one-handed application

    quick drying hand sanitizer

    nourishing aloe + vitamin E

    8 Fl.Oz. 237 mL

    A Brand By PHARMAPACKS

    container label

  • INGREDIENTS AND APPEARANCE
    CLEAR HANI-TIZER 
    alcohol liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:73599-002
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL70 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    DIISOPROPYL SEBACATE (UNII: J8T3X564IH)  
    WATER (UNII: 059QF0KO0R)  
    CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)  
    ISOPROPYL ALCOHOL (UNII: ND2M416302)  
    TOCOPHEROL (UNII: R0ZB2556P8)  
    ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)  
    AMINOMETHYLPROPANOL (UNII: LU49E6626Q)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:73599-002-08237 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product03/05/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333E01/22/2020
    Labeler - PHARMAPACKS, LLC (079254738)
    Establishment
    NameAddressID/FEIBusiness Operations
    Central Solutions Inc007118524manufacture(73599-002)
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