ZEP INSTANT HAND SANITIZER (ETHANOL) LIQUID [ZEP INC.]

ZEP INSTANT HAND SANITIZER (ETHANOL) LIQUID [ZEP INC.]
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NDC 66949-246-15, 66949-878-00, 66949-878-05, 66949-878-21
Set ID bd7e3d4f-b397-4f39-9692-1a13f232eb71
Category HUMAN OTC DRUG LABEL
Packager Zep Inc.
Generic Name
Product Class
Product Number
Application Number PART333A
  • Active Ingredient

    Alcohol 60%

  • Purpose

    Antiseptic

  • Uses

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

    

    • Flammable. Keep away from fire, flame or spark. For external use only.

    . Do not use in the eye; if in eyes, rinse thoroughly with water.

  • When using this product

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

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

  • Keep out of reach of children and pets

    Keep out of reach of children and pets. Children must be supervised in the 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

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

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

  • Questions or comments?

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

  • PRINCIPAL DISPLAY PANEL

    878_1246878_0878

  • INGREDIENTS AND APPEARANCE
    ZEP INSTANT HAND SANITIZER 
    ethanol liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:66949-878
    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:66949-878-016000 mL in 1 CASE; Type 0: Not a Combination Product01/29/200412/31/2021
    2NDC:66949-878-066000 mL in 1 CASE; Type 0: Not a Combination Product01/29/2004
    3NDC:66949-878-2415140 mL in 1 CASE; Type 0: Not a Combination Product01/29/200412/31/2021
    4NDC:66949-878-891040988 mL in 1 CONTAINER; Type 0: Not a Combination Product01/29/200412/31/2021
    5NDC:66949-878-3518927 mL in 1 PAIL; Type 0: Not a Combination Product01/29/2004
    6NDC:66949-878-872366 mL in 1 CASE; Type 0: Not a Combination Product01/29/2004
    7NDC:66949-878-142840 mL in 1 CASE; Type 0: Not a Combination Product01/29/200412/31/2021
    8NDC:66949-878-3211400 mL in 1 CASE; Type 0: Not a Combination Product01/29/200412/31/2021
    9NDC:66949-878-85208198 mL in 1 DRUM; Type 0: Not a Combination Product01/29/2004
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A01/29/2004
    ZEP INSTANT HAND SANITIZER 
    ethanol liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:66949-246
    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:66949-246-164800 mL in 1 CASE; Type 0: Not a Combination Product01/29/200412/31/2021
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A01/29/200412/31/2021
    Labeler - Zep Inc. (030471374)
    Establishment
    NameAddressID/FEIBusiness Operations
    Zep Inc.112125310manufacture(66949-878, 66949-246)

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