Label: ZEP ALCOHOL SANITIZER- alcohol liquid 

  • NDC Code(s): 66949-900-00, 66949-900-21
  • Packager: Zep Inc.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph not final

NOTE: Most over the counter (OTC) are not reviewed and approved by the FDA. However, they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Drug Label Information

Updated 12/13

If you are a consumer or patient please visit this version.

  • Active ingredient

    Alcohol 62%

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  • Purpose

    Antiseptic

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  • Uses

    • Hand sanitizing to decrease bacteria on skin.
    • No rinsing required.
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  • Warnings

    For external use only.

    Flammable. Keep away from fire, flame or spark.

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  • WHEN USING

    When using this product

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

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

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  • KEEP OUT OF REACH OF CHILDREN

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

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  • ASK DOCTOR

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

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  • Directions

    • Wet hands thoroughly with spray mist.
    • Rub hands together allowing liquid to contact all areas, especially around the nails and cuticles.
    • Continue rubbing vigorously until hands are dry.
    • No rinsing or toweling is required.
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  • Other information

    • Store at 20 to 25°C (68 to 77°F).
    • Dispose in accordance with all applicable federal, state and local regulations.
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  • Inactive ingredients

    Water, Glycerine

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  • Questions or comments?

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

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  • INGREDIENTS AND APPEARANCE
    ZEP ALCOHOL SANITIZER 
    ethanol liquid
    Product Information
    Product Type HUMAN OTC DRUG LABEL Item Code (Source) NDC:66949-900
    Route of Administration TOPICAL DEA Schedule     
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    ALCOHOL (ALCOHOL) ALCOHOL 6.2 mL  in 10 mL
    Inactive Ingredients
    Ingredient Name Strength
    WATER  
    GLYCERIN  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:66949-900-00 1000 mL in 1 BOTTLE, PLASTIC
    2 NDC:66949-900-21 3785 mL in 1 BOTTLE, PLASTIC
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC monograph not final part333A 08/07/2000
    Labeler - Zep Inc. (030471374)
    Establishment
    Name Address ID/FEI Business Operations
    Zep Inc. 030471374 manufacture(66949-900)
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