Label: EZFOAM FOAMING ALCOHOL HAND SANITIZER- foaming hand sanitizer solution

  • NDC Code(s): 50865-688-03, 50865-688-09, 50865-688-17, 50865-688-24, view more
    50865-688-41, 50865-688-50, 50865-688-78, 50865-688-91
  • Packager: Kutol Products Company
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 18, 2024

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  • ACTIVE INGREDIENT

    Ethyl Alcohol 62% v/v.......Antibacterial Agent

  • INACTIVE INGREDIENT

    Water, AMP-C8-18 Perfluoroalkylethyl Phosphate, Glycerin.

  • PURPOSE

    Hand Sanitizer to help reduce bacteria on the skin that could cause disease. Recommended for repeated use.

  • WARNINGS

    For external use only.

    FLAMMABLE. Keep away from heat or flames.

    Avoid contact with eyes. If eye contact occurs, flush with water.

    Stop use if, in rare instances, redness or irritation develop. If condition persists for more than 72 hours, consult a physician.

    Keep out of reach of children. If swallowed, contact a physician or poison control center.

  • DOSAGE & ADMINISTRATION

    To decrease bacteria on skin, apply small amount to palm. Briskly rub, covering hands with product until dry.

  • INDICATIONS & USAGE

    Hand sanitizer to help reduce bacteria on the skin that could cause disease. Recommended for repeated use.

    Avoid contact with eyes. If eye contact occurs, flush with water.

    Stop use if, in rare instances, redness or irritation develop. If condition persists for more than 72 hours, consult a physician.

    Keep out of reach of children. If swallowed, contact a physician or poison control center.

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children. If swallowed, contact a physician or poison control center.

  • PRINCIPAL DISPLAY PANEL

    Principal Display

  • INGREDIENTS AND APPEARANCE
    EZFOAM FOAMING ALCOHOL HAND SANITIZER 
    foaming hand sanitizer solution
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:50865-688
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL62 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    AMINOMETHYLPROPANOL (PERFLUORO-C6-C12 ETHYL)PHOSPHATE (UNII: QCD5R22RNT)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:50865-688-03213125 mL in 1 DRUM; Type 0: Not a Combination Product06/27/201301/21/2016
    2NDC:50865-688-093785 mL in 1 JUG; Type 0: Not a Combination Product06/27/2013
    3NDC:50865-688-1750 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product06/27/2013
    4NDC:50865-688-241000 mL in 1 BAG; Type 0: Not a Combination Product06/27/2013
    5NDC:50865-688-411000 mL in 1 BAG; Type 0: Not a Combination Product06/27/2013
    6NDC:50865-688-78950 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product06/27/2013
    7NDC:50865-688-91532 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product06/27/201301/21/2016
    8NDC:50865-688-501200 mL in 1 BAG; Type 0: Not a Combination Product06/27/2013
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)06/27/2013
    Labeler - Kutol Products Company (004236139)
    Registrant - Kutol Products Company. (004236139)
    Establishment
    NameAddressID/FEIBusiness Operations
    Kutol Products Company004236139manufacture(50865-688)
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