Label: BODY WASH- triclosan liquid

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph not final

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 August 8, 2014

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  • Back Panel Claims

    Antibacterial Moisturizing Body Wash

    Experience a whole new feeling of invigorating freshness with Antibacterial Moisturizing Body Wash.  Enjoy the tantalizing fragrance of our moisturizing, antibacterial formula that will caress your skin and leave it soft and clean.

  • Active ingredient

    Benzalkonium Chloride 0.13%

  • Purpose

    Antibacterial

  • Use

    To decrease bacteria on the skin

  • Warnings

    For external use only

  • When using this product

    • do not get into eyes.  If contact occurs, rinse thoroughly with water.
  • Keep out of reach of children

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

  • Directions

    • work a small amount into a lather
    • scrub thoroughly
    • rinse
  • Inactive ingredients

    water, PEG-120 methyl glcose dioleate, cetrimonium chloride glycerin, lauramidopropylamine oxide, cocamide MEA, fragrance, sodium sulfate, myristamidopropylamine oxide,  sodium chloride, citric acid, tetrasodium EDTA, methylchloroisothiazolinone, methylisotiazolinone, blue 1, red 33

  • Adverse Reactions

    DISTRIBUTED BY PUBLIX SUPER MARKETS, INC

    3300 PUBLIX CORPORATE PARKWAY

    LAKELAND, FL 33811

    publix.com

    Publix Guarantee: Complete satisfaction or your money back

  • Principal Display Panel

    Publix

    antibacterial

    moisturizing

    body wash

    Antibacterial Cleanser

    Plus Moisturizer

    21 FL OZ (621 mL)

    image description

  • INGREDIENTS AND APPEARANCE
    BODY WASH 
    triclosan liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:56062-945
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE1.5 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    water (UNII: 059QF0KO0R)  
    PEG-120 METHYL GLUCOSE DIOLEATE (UNII: YM0K64F20V)  
    CETRIMONIUM CHLORIDE (UNII: UC9PE95IBP)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    LAURAMIDOPROPYLAMINE OXIDE (UNII: I6KX160QTV)  
    COCO MONOETHANOLAMIDE (UNII: C80684146D)  
    SODIUM SULFATE (UNII: 0YPR65R21J)  
    MYRISTAMIDOPROPYLAMINE OXIDE (UNII: 3HSF539C9T)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    EDETATE SODIUM (UNII: MP1J8420LU)  
    METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)  
    METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)  
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    D&C RED NO. 33 (UNII: 9DBA0SBB0L)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:56062-945-56621 mL in 1 BOTTLE, PLASTIC
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A12/04/2009
    Labeler - Publix Super Markets, Inc. (006922009)
    Registrant - Vi-Jon (790752542)
    Establishment
    NameAddressID/FEIBusiness Operations
    Vi-Jon088520668manufacture(56062-945)
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