Label: WHISKCARE 371- alcohol spray

  • NDC Code(s): 65585-372-01, 65585-372-02, 65585-372-03, 65585-372-04, view more
    65585-372-05, 65585-372-06, 65585-372-07, 65585-372-08, 65585-372-09, 65585-372-10, 65585-372-11, 65585-372-12
  • Packager: Whisk Products, Inc.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated February 22, 2024

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  • 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, flush eyes with water and contact a doctor immediately.

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

    KEEP OUT OF REACH OF CHILDREN.

  • Directions

    • Dispense a small amount of spray onto the hands.
    • Spread on hands and rub into skin until dry.
    • Dispense 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 product label

  • INGREDIENTS AND APPEARANCE
    WHISKCARE 371 
    alcohol spray
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:65585-372
    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
    GLYCERIN (UNII: PDC6A3C0OX)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    WATER (UNII: 059QF0KO0R)  
    Product Characteristics
    Colorwhite (water white - colorless, dispensed as a spray) Score    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65585-372-018 in 1 BOX01/15/2008
    11 L in 1 BAG; Type 0: Not a Combination Product
    2NDC:65585-372-023.785 L in 1 BAG; Type 0: Not a Combination Product01/15/200801/15/2008
    3NDC:65585-372-0324 in 1 BOX08/18/2008
    30.118 L in 1 BOTTLE, PUMP; Type 0: Not a Combination Product
    4NDC:65585-372-04208.2 L in 1 DRUM; Type 0: Not a Combination Product03/20/2020
    5NDC:65585-372-051041 L in 1 CONTAINER, FLEXIBLE INTERMEDIATE BULK; Type 0: Not a Combination Product04/02/2020
    6NDC:65585-372-0612 in 1 BOX04/03/2020
    60.8 L in 1 BAG; Type 0: Not a Combination Product
    7NDC:65585-372-076 in 1 BOX06/04/2020
    71 L in 1 BAG; Type 0: Not a Combination Product
    8NDC:65585-372-0812 in 1 BOX06/17/2020
    80.237 L in 1 BOTTLE, PUMP; Type 0: Not a Combination Product
    9NDC:65585-372-098 in 1 BOX08/23/2021
    91 L in 1 BAG; Type 0: Not a Combination Product
    10NDC:65585-372-1012 in 1 BOX09/15/2023
    100.4 L in 1 BAG; Type 0: Not a Combination Product
    11NDC:65585-372-113.785 L in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product01/15/2008
    12NDC:65585-372-124 in 1 BOX02/22/2024
    121 L in 1 BAG; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)01/15/2008
    Labeler - Whisk Products, Inc. (834270639)
    Establishment
    NameAddressID/FEIBusiness Operations
    Whisk Products,Inc.834270639pack(65585-372) , label(65585-372)
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