Label: ZEP PROFESSIONAL ALCOHOL HAND SANITIZING - alcohol liquid 

  • Label RSS
  • NDC Code(s): 66949-109-00, 66949-109-01, 66949-109-24
  • 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 60%

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  • Purpose

    Antiseptice

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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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  • ASK DOCTOR

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

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  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children and pets.

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  • Directions

    • Use pump and apply gel to hands
    • Rub hands together allowing liquid to contact all areas, especially around the nails and cuticles.
    • Continue rubbing vigorously until hands are dry.
    • No rinsing allowed 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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  • Inactiv ingredients

    deionized water, acrylates/C10-30 alkyl acrylate crosspolymer, diisopropanolamine, fragrance

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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 PROFESSIONAL ALCOHOL HAND SANITIZING 
    ethanol liquid
    Product Information
    Product Type HUMAN OTC DRUG LABEL Item Code (Source) NDC:66949-109
    Route of Administration TOPICAL DEA Schedule     
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    ALCOHOL (ALCOHOL) ALCOHOL 6.0 mL  in 10 mL
    Inactive Ingredients
    Ingredient Name Strength
    WATER  
    CARBOMER 934  
    DIISOPROPANOLAMINE  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:66949-109-00 500 mL in 1 BOTTLE, PLASTIC
    2 NDC:66949-109-01 1000 mL in 1 BOTTLE, PLASTIC
    3 NDC:66949-109-24 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 04/07/2009
    Labeler - Zep Inc. (030471374)
    Establishment
    Name Address ID/FEI Business Operations
    Zep Inc. 030471374 manufacture(66949-109)
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