Label: AP HANSAN- alcohol spray

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 7, 2023

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

  • ​Active Ingredient

    Ethyl Alcohol 60% v/v

  • Purpose

    Skin Sanitizer

  • ​Use

    To help reduce the amount of bacteria on the skin

  • ​Warnings

    Flammable.  Keep away from fire or flame.

    For external use only.  If swallowed seek medical attention.

    When using this product do not use around or near the eyes.  If contact occurs, flus eyes iwth water and contact doctor immediately.

    Stop use and consult a doctor when skin irritation appears and lasts.

    Keep out of reach of children.

  • ​Directions

    • Place a small amount of spray into the hands.
    • Spread on hands and rub into skin until dry.
    • Place a smaller amount in one hand and spread over both hands and wrists.
    • Rub into skin until dry.
    • Children should be supervised while using this product.

  • ​Inactive Ingredients

    Water, Glycerin, Propylene Glycol

  • PRINCIPAL DISPLAY PANEL

    1 Gallon ShortNeck Bottle Label

  • INGREDIENTS AND APPEARANCE
    AP HANSAN 
    alcohol spray
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:65585-580
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL600 mL  in 1 L
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    Product Characteristics
    Colorwhite (water-white (colorless)) Score    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65585-580-013.785 L in 1 BOTTLE; Type 0: Not a Combination Product10/24/2016
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)10/24/2016
    Labeler - WhiskProducts, Inc. (834270639)
    Establishment
    NameAddressID/FEIBusiness Operations
    Whisk Products, Inc.834270639label(65585-580) , pack(65585-580)