ZEP PROFESSIONAL ALCOHOL HAND SANITIZING (ETHANOL) LIQUID [ZEP INC.]

ZEP PROFESSIONAL ALCOHOL HAND SANITIZING (ETHANOL) LIQUID [ZEP INC.]
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NDC 66949-109-00, 66949-109-01, 66949-109-24
Set ID 961024fe-5714-4fad-9481-de823bac67b8
Category HUMAN OTC DRUG LABEL
Packager Zep Inc.
Generic Name
Product Class
Product Number
Application Number PART333A
  • Active ingredient

    Ethanol 60%

  • Purpose

    Antiseptic

  • Uses

    • Hand sanitizing to decrease bacteria on skin.
    • Recommended for repeated use.
    • No rinsing required.
  • Warnings

    For external use only.

    Flammable. Keep away from fire, flame or spark.

    Do not use in eyes; if in eyes, rince thoroughly with water.

  • WHEN USING

    When using this product

    • Do not swallow.
    • If swallowed, do not induce vomiting and if individual is conscious, give large quantities of water to drink and consult a physician immediately.
  • 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.

  • 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 or toweling is required.
  • Other information

    • Keep container closed and stored in a dry area at temperatures between 40°F and 120°F.
    • Do not reuse empty container.
    • Dispose in accordance with all applicable federal, state & local regulations.
  • Inactiv ingredients

    Deionized Water, Diisopropanolamine, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Fragrance

  • Questions or comments?

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

  • PRINCIPAL DISPLAY PANEL

    r109.jpg

  • INGREDIENTS AND APPEARANCE
    ZEP PROFESSIONAL ALCOHOL HAND SANITIZING 
    ethanol liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:66949-109
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL60 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    CARBOMER INTERPOLYMER TYPE A (55000 CPS) (UNII: 59TL3WG5CO)  
    DIISOPROPANOLAMINE (UNII: 0W44HYL8T5)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:66949-109-011000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product04/07/200912/31/2021
    2NDC:66949-109-243785 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product04/07/200912/31/2021
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A04/07/200912/31/2021
    Labeler - Zep Inc. (030471374)
    Establishment
    NameAddressID/FEIBusiness Operations
    Zep Inc.112125310manufacture(66949-109)

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