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Zep Cherry Creme (Zep Inc.)

Available Formats

Dosage Form Package Information Links
LIQUID 3785 mL in 1 BOTTLE, PLASTIC (66949-898-24) Label Information
LIQUID 500 mL in 1 BOTTLE, PLASTIC (66949-898-00) Label Information
LIQUID 1000 mL in 1 BOTTLE, PLASTIC (66949-898-10) Label Information

Complete Zep Cherry Creme Information

  • Active ingredient

    Triclosan 0.1%


  • Purpose

    Antimicrobial


  • Uses

    For handwashing to decrease bacteria on skin.


  • Warnings

    For external use only.


  • WHEN USING

    When using this product

    • if swallowed, seek medical attention.
    • if eye contact occurs, flush eyes with water and contact a physicican.

  • STOP USE

    Stop use and ask doctor if skin irritation develops.


  • KEEP OUT OF REACH OF CHILDREN

    Except under adult supervision,  keep out of reach of children.


  • Directions

    • Press pump to dispense product onto hands, lather and rinse.

  • Other information

    • Store at room temperature.
    • Do not freeze.

  • Inactive ingredients

    Water, Sodium Lauryl Sulfate, Cocomidopropyl Betaine, Cocamide DIPA, Glycol Stearate, Cocamidopropyl PG-Dimonium Chloride Phosphate, Glycerin, Tetrasodium EDTA, Fragrance, Citric Acid, Methylchloroisothiazolinone (and) Methylisothiazolinone, Glutaral, Sodium Xylenesulfonate, Sodium Chloride, Red 4, Red 33


  • INGREDIENTS AND APPEARANCE
    ZEP CHERRY CREME 
    triclosan liquid
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:66949-898
    Route of Administration TOPICAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    TRICLOSAN (UNII: 4NM5039Y5X) (TRICLOSAN - UNII:4NM5039Y5X) TRICLOSAN 0.01 g  in 10 mL
    Inactive Ingredients
    Ingredient Name Strength
    WATER (UNII: 059QF0KO0R)  
    SODIUM LAURYL SULFATE (UNII: 368GB5141J)  
    COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)  
    COCO DIISOPROPANOLAMIDE (UNII: S485AM948Q)  
    GLYCOL STEARATE (UNII: 0324G66D0E)  
    COCAMIDOPROPYL PG-DIMONIUM CHLORIDE PHOSPHATE (UNII: H2KVQ74JM4)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
    METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)  
    METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)  
    GLUTARAL (UNII: T3C89M417N)  
    SODIUM XYLENESULFONATE (UNII: G4LZF950UR)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    FD&C RED NO. 4 (UNII: X3W0AM1JLX)  
    D&C RED NO. 33 (UNII: 9DBA0SBB0L)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:66949-898-24 3785 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 02/26/2003 01/01/2020
    2 NDC:66949-898-00 500 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 02/26/2003 01/01/2020
    3 NDC:66949-898-10 1000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 02/26/2003 01/01/2020
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC monograph not final part333A 02/26/2003 01/01/2020
    Labeler - Zep Inc. (030471374)
    Establishment
    Name Address ID/FEI Business Operations
    Zep Inc. 030471374 manufacture(66949-898)