Label: HAND SANITIZER FOAM- alcohol solution

  • NDC Code(s): 77955-002-02
  • Packager: Custom Chemical Solutions
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated January 22, 2024

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  • Active ingredients (v/v)

    Ethyl Alcohol 70%

  • Purpose

    Antimicrobial

  • Uses

    • To decrease bacteria on the skin that could cause disease
    • Recommended for repeated use
  • Warnings

    For external use only: hands

    Flammable. Keep away from fire or flame.

    When using this productavoid contact with eyes.

    In case of eye contact, flush eyes with water.

    Avoid contact with broken skin.

    Do not ingest or inhale.

    Stop use and ask a doctorif irritation or redness develops, or if condition persists for more than 72 hours.

    Keep out of reach of children.

    If swallowed, get medical help or contact a Poison Control Center right away.

  • Directions:

    Pump enough product into palm of hand to thoroughly cover all surfaces of both hands.

    Rub hands together briskly until dry.

    For children under 6, use only under adult supervision.

  • Other information:

    Store below 110 F (43 C).

    May discolor some fabrics.

    May be harmful to wood finishes and plastics.

  • Inactive ingredients:

    Water (Eau), Bis-PEG-10 Dimethicone, Glycerin, Isopropyl Myristate, Tocopheryl Acetate, Denatonium Benzoate

  • PRINCIPAL DISPLAY PANEL

    container labelHSF1

    HAND

    SANITIZER

    FOAM

    UniFirst Corporation 88UF 1L (1000 mL, 33.8 US fl. oz.)

  • INGREDIENTS AND APPEARANCE
    HAND SANITIZER FOAM 
    alcohol solution
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:77955-002
    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
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    WATER (UNII: 059QF0KO0R)  
    ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)  
    DENATONIUM BENZOATE (UNII: 4YK5Z54AT2)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    BIS-PEG-10 DIMETHICONE/DIMER DILINOLEATE COPOLYMER (UNII: CF5W1YCX11)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:77955-002-021000 mL in 1 BOTTLE; Type 0: Not a Combination Product10/05/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)10/05/2020
    Labeler - Custom Chemical Solutions (081096319)
    Establishment
    NameAddressID/FEIBusiness Operations
    Kutol Products Company004236139manufacture(77955-002)
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