Label: BOBBARKER ANTIBACTERIAL WRAPPED BODY- benzethonium chloride soap

  • NDC Code(s): 72797-001-01, 72797-001-02, 72797-001-03, 72797-001-04
  • Packager: Yangzhou H&R Plastic Daily Chemical Co., Ltd.
  • 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 January 13, 2023

If you are a consumer or patient please visit this version.

  • Active Ingredient

    Benzethonium Chloride 0.1%

  • Purpose

    Antibacterial

  • Uses

    for washing to decrease bacteria on the skin.

  • Warnings

    For external use only.

  • When using this product

    Avoid contact with eyes. In case of eye contact, flush with water.

    Don't use this product on infants under 6 months of age.

  • Stop use and ask a doctor

    If irritation and redness develops.

  • Keep out of reach of children.

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

  • Directions

    • wet bar with water
    • lather vigorously and wash skin
    • rinse and dry thoroughly.
  • Inactive Ingredients

    Soap (Sodium Palmate and/or Sodium Tallowate, Sodium Cocoate and/or Sodium Palm Kernelate), Water, Palm Acid, Glycerin, Sodium Chloride, Coconut Acid, Fragrance, Tetrasodium EDTA, Citric Acid Anhydrous

  • PRINCIPAL DISPLAY PANEL

    label image

  • INGREDIENTS AND APPEARANCE
    BOBBARKER ANTIBACTERIAL WRAPPED BODY 
    benzethonium chloride soap
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:72797-001
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZETHONIUM CHLORIDE (UNII: PH41D05744) (BENZETHONIUM - UNII:1VU15B70BP) BENZETHONIUM CHLORIDE0.1 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    PALM ACID (UNII: B6G0Y5Z616)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    COCONUT ACID (UNII: 40U37V505D)  
    SODIUM PALMATE (UNII: S0A6004K3Z)  
    SODIUM COCOATE (UNII: R1TQH25F4I)  
    SODIUM PALM KERNELATE (UNII: 6H91L1NXTW)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:72797-001-011000 in 1 BOX01/13/2023
    111.06 g in 1 PACKAGE; Type 0: Not a Combination Product
    2NDC:72797-001-02500 in 1 BOX01/13/2023
    229.78 g in 1 PACKAGE; Type 0: Not a Combination Product
    3NDC:72797-001-03144 in 1 BOX01/13/2023
    381.04 g in 1 PACKAGE; Type 0: Not a Combination Product
    4NDC:72797-001-04144 in 1 BOX01/13/2023
    485.07 g in 1 PACKAGE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333E01/13/2023
    Labeler - Yangzhou H&R Plastic Daily Chemical Co., Ltd. (554455648)
    Establishment
    NameAddressID/FEIBusiness Operations
    Yangzhou H&R Plastic Daily Chemical Co., Ltd.554455648manufacture(72797-001)