Label: WHISKCARE 373- alcohol soap

  • NDC Code(s): 65585-374-01, 65585-374-02, 65585-374-03, 65585-374-04, view more
    65585-374-05, 65585-374-06, 65585-374-07, 65585-374-08, 65585-374-09, 65585-374-10, 65585-374-11
  • Packager: Whisk Products, Inc.
  • Category: HUMAN OTC DRUG LABEL

Drug Label Information

Updated December 1, 2023

If you are a healthcare professional or from the pharmaceutical industry please visit this version.

View All Sections
  • Active Ingredient

    Ethyl Alcohol 62% 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

    • Pump a small amount of foam into palm of hand.
    • Spread on hands and rub into skin until dry.
    • Place a smaller amount into one hand and spread over both hands and wrists.
    • Run into skin until dry.
    • Children should be supervised while using this product.
  • Inactive Ingredients

    Water, Acrylates/Perfluorohexylethyl Methacrylate Copolymer, Perfluorohexylethyl Alcohol, Glycerin, Aloe Barbadensis Leaf Juice

  • PRINCIPAL DISPLAY PANEL

    1 Gallon Product Label

  • INGREDIENTS AND APPEARANCE
    WHISKCARE 373 
    alcohol soap
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:65585-374
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL620 mL  in 1 L
    Inactive Ingredients
    Ingredient NameStrength
    BUTYL ACRYLATE/METHYL METHACRYLATE/PERFLUOROHEXYLETHYL METHACRYLATE COPOLYMER (SALUS AF) (UNII: HLB263IJK9)  
    2-(PERFLUOROHEXYL)ETHANOL (UNII: G2R5YO5N3V)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    WATER (UNII: 059QF0KO0R)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    Product Characteristics
    Colorwhite (water white - colorless, dispensed as white foam) Score    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65585-374-018 in 1 BOX06/17/2022
    11 L in 1 BAG; Type 0: Not a Combination Product
    2NDC:65585-374-023.785 L in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product06/17/2022
    3NDC:65585-374-036 in 1 BOX06/17/202206/17/2022
    30.55 L in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product
    4NDC:65585-374-096 in 1 BOX06/17/2022
    40.55 L in 1 BOTTLE, PUMP; Type 0: Not a Combination Product
    5NDC:65585-374-043 in 1 BOX06/17/202207/31/2023
    51 L in 1 BAG; Type 0: Not a Combination Product
    6NDC:65585-374-054 in 1 BOX06/17/2022
    61 L in 1 BAG; Type 0: Not a Combination Product
    7NDC:65585-374-060.05 L in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product06/17/202206/17/2022
    8NDC:65585-374-100.05 L in 1 BOTTLE, PUMP; Type 0: Not a Combination Product06/17/2022
    9NDC:65585-374-0724 in 1 BOX06/17/202206/17/2022
    90.05 L in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product
    10NDC:65585-374-1124 in 1 BOX06/17/2022
    100.05 L in 1 BOTTLE, PUMP; Type 0: Not a Combination Product
    11NDC:65585-374-084 in 1 BOX06/17/202207/31/2024
    111 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)06/17/2022
    Labeler - Whisk Products, Inc. (834270639)
    Establishment
    NameAddressID/FEIBusiness Operations
    Whisk Products, Inc.834270639label(65585-374) , pack(65585-374)
View All Sections

Find additional resources

(also available in the left menu)

Safety

Report Adverse Events, FDA Safety Recalls, Presence in Breast Milk

Related Resources

Medline Plus, Clinical Trials

More Info on this Drug

Get Label RSS Feed, View NDC Code(s)NEW!