Label: ANTIMICROBIAL FACE BODY WASH- benzethonium chloride liquid liquid

  • NDC Code(s): 37945-902-08
  • Packager: Bio-Medical & Pharmaceutical Manufacturing Corporation
  • 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 April 15, 2020

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  • Drug Facts

    Antimicrobial Wash

  • Active Ingredients

    Benzethonium Chloride 0.2%

  • Purpose

    Antimicrobial

  • Use

    A unique, non-drying cleanser.
    Developed for all skin types and pH balanced.
    Helps to decrease bacteria on the skin.

  • Warnings

    External use only.
    Do not use in eyes.
    In case of deep wounds or puncture wounds, consult a physician.
    If irritation develops and persists for more than a few days, discontinue use and consult a physician.

  • Keep out of reach of children

    If swallowed, get medical help or contact a Poison Control Center immediately. (1-800-222-1222)

  • Directions

    Wet hands and other areas to be treated.
    Place a small amount of gel in your hands and work into lather.
    Apply lather to areas to be treated using a gentle, circular motion.

    Rinse clean.

  • Other information

    Alcohol Free

    Moisturizes

    Made In USA

  • Inactive Ingredients

    Purified Water, Ammonium Lauryl Sulfate, Lauramidopropyl Betaine, Hydroxypropyl Bis- Hydroxyethyldimonium Chloride, Propylene Glycol, Hydroxypropylmethylcellulose, Sodium Chloride, Diazolidinyl Urea, PEG-4 Laurate, Methylparaben, Propylparaben, 3-iodo-2-propynylbutylcarbamate.

  • Questions or Comments

    Bio-Medical & Pharm. Mfg. Corp.

    4311 South Dr.,

    Houston, TX 77053-4820

    Phone: 281.835.8051

  • PRINCIPAL DISPLAY PANEL

    Label

  • INGREDIENTS AND APPEARANCE
    ANTIMICROBIAL FACE BODY WASH 
    benzethonium chloride liquid liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:37945-902
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZETHONIUM CHLORIDE (UNII: PH41D05744) (BENZETHONIUM - UNII:1VU15B70BP) BENZETHONIUM CHLORIDE0.2 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    LAURAMIDOPROPYL BETAINE (UNII: 23D6XVI233)  
    PEG-4 LAURATE (UNII: AYF4VM3N1Z)  
    AMMONIUM LAURYL SULFATE (UNII: Q7AO2R1M0B)  
    PROPYLPARABEN (UNII: Z8IX2SC1OH)  
    IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB)  
    HYPROMELLOSES (UNII: 3NXW29V3WO)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    WATER (UNII: 059QF0KO0R)  
    HYDROXYPROPYL BIS-HYDROXYETHYLDIMONIUM CHLORIDE (UNII: 1EO3O1X7HG)  
    METHYLPARABEN (UNII: A2I8C7HI9T)  
    DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:37945-902-08236 g in 1 BOTTLE; Type 0: Not a Combination Product10/09/2015
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333E10/09/2015
    Labeler - Bio-Medical & Pharmaceutical Manufacturing Corporation (072186356)
    Establishment
    NameAddressID/FEIBusiness Operations
    Bio-Medical & Pharmaceutical Manufacturing Corporation072186356manufacture(37945-902)
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