Home > Drugs A-Z > DebMed Antimicrobial Body Wash and Shampoo

DebMed Antimicrobial Body Wash and Shampoo (Deb USA, Inc.)

Available Formats

Dosage Form Package Information Links
LIQUID 1000 mL in 1 BOTTLE, PLASTIC (11084-061-27) Label Information
LIQUID 222 mL in 1 BOTTLE, PLASTIC (11084-061-38) Label Information

Complete DebMed Antimicrobial Body Wash and Shampoo Information

  • ACTIVE INGREDIENT

    Active ingredient

    Triclosan, 0.70%


  • PURPOSE

    Purpose

    Antimicrobial


  • INDICATIONS & USAGE

    Uses

    For hand and body washing to reduce bacteria on the skin


  • WARNINGS

    Warnings

    For external use only

    When using this product avoid contact with eyes.  In case of eye contact, flush with water

    Keep out of reach of children

    If swallowed, get medical help or contact a Poison Control Center right away.


  • DOSAGE & ADMINISTRATION

    Directions

    Apply product onto washcloth or directly onto skin

    Lather and wash for 15-20 seconds

    Rinse and dry thoroughly


  • INACTIVE INGREDIENT

    Inactive ingredients

    Water, Disodium Laureth Sulfosuccinate, Sodium Laureth Sulfate, TEA-Dodecylbenzene Sulfonate, Citric Acid, Phenoxyethanol, Hyroxypropyl Guar Hydroxypropyltrimonium Chloride, Aloe Barbadensis Leaf Juice, Sodium Benzoate, Allantoin, Sodium Chloride, Tetrasodium EDTA, Potassium Sorbate, Fragrance, Yellow 5 (CI19140), Red 40 (CI 16035), Blue 1 (CI 42090).


  • PRINCIPAL DISPLAY PANEL

    DebMed Engineering Hand Hygiene Compliance

    AntiMicrobial Body Wash and Shampoo

    1L

    33.8 fl oz

    Made in USA

    DMABHB1L

    container label


  • INGREDIENTS AND APPEARANCE
    DEBMED ANTIMICROBIAL BODY WASH AND SHAMPOO 
    triclosan liquid
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:11084-061
    Route of Administration TOPICAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    Triclosan (UNII: 4NM5039Y5X) (Triclosan - UNII:4NM5039Y5X) Triclosan 0.70 mL  in 100 mL
    Inactive Ingredients
    Ingredient Name Strength
    WATER (UNII: 059QF0KO0R)  
    DISODIUM LAURETH SULFOSUCCINATE (UNII: D6DH1DTN7E)  
    TEA-DODECYLBENZENESULFONATE (UNII: 8HM7ZD48HN)  
    SODIUM LAURETH SULFATE (UNII: BPV390UAP0)  
    ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    EDETATE SODIUM (UNII: MP1J8420LU)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    GUAR GUM (UNII: E89I1637KE)  
    ALLANTOIN (UNII: 344S277G0Z)  
    FD&C RED NO. 40 (UNII: WZB9127XOA)  
    FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
    SODIUM BENZOATE (UNII: OJ245FE5EU)  
    POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:11084-061-27 1000 mL in 1 BOTTLE, PLASTIC
    2 NDC:11084-061-38 222 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 07/01/2011
    Labeler - Deb USA, Inc. (607378015)
    Establishment
    Name Address ID/FEI Business Operations
    Deb USA, Inc. 607378015 manufacture
    Establishment
    Name Address ID/FEI Business Operations
    Deb Worldwide Healthcare Inc. 205662831 manufacture