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Panache (Deb USA, Inc.)

Available Formats

Dosage Form Package Information Links
LIQUID 3780 mL in 1 BOTTLE, PLASTIC (11084-115-05) Label Information
LIQUID 118 mL in 1 BOTTLE, PLASTIC (11084-115-34) Label Information
LIQUID 1000 mL in 1 CARTRIDGE (11084-115-27) Label Information
LIQUID 2000 mL in 1 CARTRIDGE (11084-115-07) Label Information

Complete Panache Information

  • ACTIVE INGREDIENT

    Active ingredient

    Triclosan 0.5%


  • PURPOSE

    Antibacterial


  • INDICATIONS & USAGE

    Uses

    For washing to decrease bacteria on the skin


  • WARNINGS

    Warnings

    For external use only

    Avoid contact with the eyes

    Keep out of reach of children

    Consult with a physician if ingested


  • DOSAGE & ADMINISTRATION

    Directions

    Dispense product onto washcloth or directly onto skin

    Lather and wash for 15-20 seconds

    Rinse thoroughly


  • INACTIVE INGREDIENT

    Water, Sodium Laureth Sulfate, Propylene Glycol, Disodium Laureth Sulfosuccinate, Sodium Chloride, Cocamide DEA, Cocamidopropyl Betaine, Fragrance, Tetrasodium EDTA, Citric Acid, Methylchloroisothiazolinone, Methylisothiazolinone, FDC Red No. 40, FDC Yellow No. 5.



  • INGREDIENTS AND APPEARANCE
    PANACHE   ANTIBACTERIAL BODY WASH
    triclosan liquid
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:11084-115
    Route of Administration TOPICAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    Triclosan (UNII: 4NM5039Y5X) (Triclosan - UNII:4NM5039Y5X) Triclosan .55 mL  in 100 mL
    Inactive Ingredients
    Ingredient Name Strength
    Water (UNII: 059QF0KO0R)  
    Sodium Laureth Sulfate (UNII: BPV390UAP0)  
    Propylene Glycol (UNII: 6DC9Q167V3)  
    Disodium Laureth Sulfosuccinate (UNII: D6DH1DTN7E)  
    Sodium Chloride (UNII: 451W47IQ8X)  
    COCO DIETHANOLAMIDE (UNII: 92005F972D)  
    Cocamidopropyl Betaine (UNII: 5OCF3O11KX)  
    Edetate Sodium (UNII: MP1J8420LU)  
    Anhydrous Citric Acid (UNII: XF417D3PSL)  
    FD&C Red No. 40 (UNII: WZB9127XOA)  
    FD&C Yellow No. 5 (UNII: I753WB2F1M)  
    Methylchloroisothiazolinone (UNII: DEL7T5QRPN)  
    Methylisothiazolinone (UNII: 229D0E1QFA)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:11084-115-34 118 mL in 1 BOTTLE, PLASTIC
    2 NDC:11084-115-27 1000 mL in 1 CARTRIDGE
    3 NDC:11084-115-07 2000 mL in 1 CARTRIDGE
    4 NDC:11084-115-05 3780 mL in 1 BOTTLE, PLASTIC
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC monograph not final part333A 01/01/2010
    Labeler - Deb USA, Inc. (607378015)
    Establishment
    Name Address ID/FEI Business Operations
    Deb USA, Inc. 607378015 manufacture