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Zep Foam San (Zep Inc.)

Available Formats

Dosage Form Package Information Links
LIQUID 1000 mL in 1 BOTTLE, PLASTIC (66949-880-10) Label Information
LIQUID 550 mL in 1 BOTTLE, PLASTIC (66949-880-03) Label Information
LIQUID 2500 mL in 1 BOTTLE, PLASTIC (66949-880-12) Label Information
LIQUID 75708 mL in 1 PACKAGE (66949-880-50) Label Information

Complete Zep Foam San Information

  • Active ingredient

    Benzethonium chloride 0.2%


  • Purpose

    Antiseptic


  • Uses

    • Kills 99.99% of most common germs that cause illness in as little as 15 seconds.
    • No rinsing required.
    • Does not contain alcohol.
    • Sanitizing to decrease bacteria on skin.

  • Warnings

    For external use only.


  • WHEN USING

    When using this product

    • Avoid eye contact.
    • If in eyes, rinse promptly and thoroughly with water.

  • STOP USE

    Stop use and ask doctor if skin irritation or redness persists for more than 72 hours.


  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children and pets. Children must be supervised in use of this product.


  • ASK DOCTOR

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


  • Directions

    • Press pump to dispense product onto hands.
    • Rub hands together allowing foam to contact all areas, especially around the nails.
    • Continue until foam had disappeared and/or hands are dry.

  • Other information

    • Store at 20 to 25C (68 to 77F).
    • Do not freeze.
    • Dispose in accordance with all applicable federal, state and local regulations.

  • Inactive ingredients

    Water, Glycerin, PEG/PPG-18/18 Dimethicone, DMDM Hydantoin (and) Iodopropynyl Butylcarbomate, Hydroxypropyl Methylcellulose


  • Questions or comments?

    Call 1-800-I-BUY-ZEP (1-800-428-9937)


  • INGREDIENTS AND APPEARANCE
    ZEP FOAM SAN 
    benzethonium chloride liquid
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:66949-880
    Route of Administration TOPICAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    BENZETHONIUM CHLORIDE (UNII: PH41D05744) (BENZETHONIUM - UNII:1VU15B70BP) BENZETHONIUM CHLORIDE 0.02 g  in 10 mL
    Inactive Ingredients
    Ingredient Name Strength
    WATER (UNII: 059QF0KO0R)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    PEG/PPG-18/18 DIMETHICONE (UNII: 9H0AO7T794)  
    DMDM HYDANTOIN (UNII: BYR0546TOW)  
    IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB)  
    HYDROXYPROPYL CELLULOSE (TYPE J) (UNII: 5Y0974F5PW)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:66949-880-03 550 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 03/18/2003
    2 NDC:66949-880-10 1000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 03/18/2003
    3 NDC:66949-880-12 2500 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 03/18/2003
    4 NDC:66949-880-50 75708 mL in 1 PACKAGE; Type 0: Not a Combination Product 03/18/2003
    5 NDC:66949-880-85 208198 mL in 1 DRUM; Type 0: Not a Combination Product 03/18/2003
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC monograph not final part333E 03/18/2003
    ZEP NON ALCOHOL FOAM SANITIZER 
    benzethonium chloride liquid
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:66949-248
    Route of Administration TOPICAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    BENZETHONIUM CHLORIDE (UNII: PH41D05744) (BENZETHONIUM - UNII:1VU15B70BP) BENZETHONIUM CHLORIDE 0.02 g  in 10 mL
    Inactive Ingredients
    Ingredient Name Strength
    WATER (UNII: 059QF0KO0R)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    PEG/PPG-18/18 DIMETHICONE (UNII: 9H0AO7T794)  
    DMDM HYDANTOIN (UNII: BYR0546TOW)  
    IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB)  
    HYDROXYPROPYL CELLULOSE (TYPE J) (UNII: 5Y0974F5PW)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:66949-248-15 550 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 07/14/2011
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC monograph not final part333E 07/14/2011
    Labeler - Zep, Inc (030471374)
    Establishment
    Name Address ID/FEI Business Operations
    Zep Inc. 030471374 manufacture(66949-880, 66949-248)