Label: ZEP PROFESSIONAL HEALTHCARE WORKER- triclosan liquid

  • Category: HUMAN OTC DRUG LABEL

DISCLAIMER: Most OTC drugs are not reviewed and approved by 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 December 5, 2013

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  • Active ingredient

    Triclosan 0.1%

  • Purpose

    Antimicrobial

  • Uses

    Hand washing to decrease bacteria on skin.

  • Warnings

    For external use only.

  • DO NOT USE

    Do not use in the eyes.

  • WHEN USING

    When using this product

    • If swallowed, seek medical attention.
    • If eye contact occurs, flush eyes with water and contact a physician.
    • Discontinue use if irritation and redness develop.
    • If condition persists for more than 72 hours, consult a doctor.
  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children.

  • Directions

    • Wet hands with water
    • Place hands under dispenser
    • Apply foamed soap
    • Massage soap into hands and wrists, emphasizing back of hands, knuckles and cuticles
    • Rinse thoroughly
  • Other information

    • Store at room temperature.
    • Do not freeze.
  • Inactive ingredients

    Water, Sodium Lauryl Sulfoacetate (and) Disodium Laurethsulfosuccinate, Sodium Cocoyl Sarcosinate, Cocamidopropyl PG-Dimonium Chloride Phosphate, Glycerine, Hexylene Glycol, PEG-75 Lanolin, Tetrasodium EDTA, Methylchloroisothiazolinone (and) Methylisothiazoline, Fragrance, Glutaral

  • PRINCIPAL DISPLAY PANEL

    r210.jpg

  • INGREDIENTS AND APPEARANCE
    ZEP PROFESSIONAL HEALTHCARE WORKER 
    triclosan liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:66949-210
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    TRICLOSAN (UNII: 4NM5039Y5X) (TRICLOSAN - UNII:4NM5039Y5X) TRICLOSAN.01 g  in 10 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    SODIUM LAURYL SULFOACETATE (UNII: D0Y70F2B9J)  
    DISODIUM LAURETH SULFOSUCCINATE (UNII: D6DH1DTN7E)  
    SODIUM COCOYL SARCOSINATE (UNII: 1R9DUY89CZ)  
    COCAMIDOPROPYL PG-DIMONIUM CHLORIDE PHOSPHATE (UNII: H2KVQ74JM4)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    HEXYLENE GLYCOL (UNII: KEH0A3F75J)  
    PEG-75 LANOLIN (UNII: 09179OX7TB)  
    METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)  
    METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)  
    GLUTARAL (UNII: T3C89M417N)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:66949-210-011000 mL in 1 BOTTLE, PLASTIC
    2NDC:66949-210-213785 mL in 1 BOTTLE, PLASTIC
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A10/05/2009
    Labeler - Zep Inc. (030471374)
    Establishment
    NameAddressID/FEIBusiness Operations
    Zep Inc.030471374manufacture(66949-210)
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