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Zep Alcohol Sanitizer (Zep Inc.)

Available Formats

Dosage Form Package Information Links
LIQUID 1000 mL in 1 BOTTLE, PLASTIC (66949-900-00) Label Information
LIQUID 3785 mL in 1 BOTTLE, PLASTIC (66949-900-21) Label Information

Complete Zep Alcohol Sanitizer Information

  • Active ingredient

    Alcohol 62%

  • Purpose

    Antiseptic

  • Uses

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

    For external use only.

    Flammable. Keep away from fire, flame or spark.

  • 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

    • 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.
  • Other information

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

    Water, Glycerine

  • Questions or comments?

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

  • INGREDIENTS AND APPEARANCE
    ZEP ALCOHOL SANITIZER 
    ethanol liquid
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:66949-900
    Route of Administration TOPICAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 6.2 mL  in 10 mL
    Inactive Ingredients
    Ingredient Name Strength
    GLYCERIN (UNII: PDC6A3C0OX)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:66949-900-00 1000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 08/07/2000
    2 NDC:66949-900-21 3785 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 08/07/2000
    3 NDC:66949-900-85 208198 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 08/07/2000
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC monograph not final part333A 08/07/2000
    ZEP ALCOHOL SANITIZER 
    ethanol liquid
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:66949-357
    Route of Administration TOPICAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 6.2 mL  in 10 mL
    Inactive Ingredients
    Ingredient Name Strength
    WATER (UNII: 059QF0KO0R)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:66949-357-15 1200 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 08/07/2000
    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. 112125310 manufacture(66949-900, 66949-357)
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