Label: BOB BARKER ANTIBACTERIAL UN-WRAPPED BODY- benzethonium chloride soap

  • NDC Code(s): 53247-118-01, 53247-118-02, 53247-118-03, 53247-118-04
  • Packager: Bob Barker Company Inc.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated October 30, 2023

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

View All Sections
  • SPL UNCLASSIFIED SECTION

    Drug Facts

  • Active Ingredient

    Benzethonium Chloride 0.1%

  • Purpose

    Antibacterial

  • Uses

    For washing to decrease bacteria on skin.

  • Warnings

    For External Use Only.

    Do not use this product on infants under 6.

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

    Stop use and ask 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

    Sodium Palmate, Calcium Carbonate, Water, Sodium Palm Kernelate, Talcum, Palm Acid, Glycerin, Sodium Chloride, Sodium Lauryl Ether Sulfate, Titanium Dioxide, Palm Kernel Acid, Fragrance, Tetrasodium EDTA, Tetrasodium Etidronate

  • PRINCIPAL DISPLAY PANEL - 500 Bar Case

    BobBarker®

    ANTIBACTERIAL UNWRAPPED BODY SOAP

    500 Bars-Total Net Weight 564.38 OZ. (35.27 LB) (16 KG)

    PRINCIPAL DISPLAY PANEL - 500 Bar Case
  • INGREDIENTS AND APPEARANCE
    BOB BARKER ANTIBACTERIAL UN-WRAPPED BODY 
    benzethonium chloride soap
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:53247-118
    Route of AdministrationCUTANEOUS
    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
    Sodium Palmate (UNII: S0A6004K3Z)  
    Calcium Carbonate (UNII: H0G9379FGK)  
    Water (UNII: 059QF0KO0R)  
    Sodium Palm Kernelate (UNII: 6H91L1NXTW)  
    Talc (UNII: 7SEV7J4R1U)  
    Palm Acid (UNII: B6G0Y5Z616)  
    Glycerin (UNII: PDC6A3C0OX)  
    Sodium Chloride (UNII: 451W47IQ8X)  
    Sodium Laureth-3 Sulfate (UNII: BPV390UAP0)  
    Titanium Dioxide (UNII: 15FIX9V2JP)  
    Palm Kernel Acid (UNII: 79P21R4317)  
    Edetate Sodium (UNII: MP1J8420LU)  
    Etidronate Tetrasodium (UNII: CZZ9T1T1X4)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:53247-118-011000 in 1 CASE06/01/2017
    111 g in 1 APPLICATOR; Type 0: Not a Combination Product
    2NDC:53247-118-02500 in 1 CASE06/01/2017
    232 g in 1 APPLICATOR; Type 0: Not a Combination Product
    3NDC:53247-118-03144 in 1 CASE06/01/2017
    375 g in 1 APPLICATOR; Type 0: Not a Combination Product
    4NDC:53247-118-04200 in 1 CASE06/01/2017
    485 g in 1 APPLICATOR; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph drugM00306/01/2017
    Labeler - Bob Barker Company Inc. (058525536)
View All Sections

Find additional resources

(also available in the left menu)

Safety

Report Adverse Events, FDA Safety Recalls, Presence in Breast Milk

Related Resources

Medline Plus, Clinical Trials, PubMed, Biochemical Data Summary

More Info on this Drug

View Labeling Archives, RxNorm, Get Label RSS Feed, View NDC Code(s)NEW!