Label: PRIME SOURCE ANTIBACTERIAL FOAM SO AP TRICLOSAN LIQUID- triclosan liquid

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: Export only

Drug Label Information

Updated November 19, 2018

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  • INGREDIENTS AND APPEARANCE
    PRIME SOURCE ANTIBACTERIAL FOAM SO AP TRICLOSAN LIQUID 
    triclosan liquid
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:66294-033
    Route of Administration TOPICAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    TRICLOSAN (UNII: 4NM5039Y5X) (TRICLOSAN - UNII:4NM5039Y5X) TRICLOSAN 0.003 mg  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    WATER (UNII: 059QF0KO0R)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    ALCOHOL (UNII: 3K9958V90M)  
    LAURIC ACID (UNII: 1160N9NU9U)  
    MONOETHANOLAMINE (UNII: 5KV86114PT)  
    DISODIUM COCOAMPHODIACETATE (UNII: 18L9G3U51M)  
    LACTIC ACID (UNII: 33X04XA5AT)  
    ISOPROPYL ALCOHOL (UNII: ND2M416302)  
    POLYETHYLENE GLYCOL 200 (UNII: R95B8J264J)  
    POLYQUATERNIUM-10 (30000 MPA.S AT 2%) (UNII: C7RDC8Y4JS)  
    SODIUM METABISULFITE (UNII: 4VON5FNS3C)  
    SODIUM SULFITE (UNII: VTK01UQK3G)  
    EDETATE SODIUM (UNII: MP1J8420LU)  
    SODIUM SULFATE (UNII: 0YPR65R21J)  
    IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:66294-033-42 1250 mL in 1 BOTTLE; Type 0: Not a Combination Product 03/15/2006
    2 NDC:66294-033-40 1200 mL in 1 BOTTLE; Type 0: Not a Combination Product 03/15/2006
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    export only 03/15/2006
    Labeler - BUNZL (799540588)
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