Label: MERIDIAN UNWRAPPED ANTIBACTERIAL DEODORANT- benzethonium chloride soap

  • NDC Code(s): 53247-137-01, 53247-137-02, 53247-137-03, 53247-137-04
  • Packager: Bob Barker Company Inc.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated October 14, 2024

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  • SPL UNCLASSIFIED SECTION

    Drug Facts

  • Active Ingredient

    Benzethonium Chloride 0.1%

  • Purpose

    Antibacterial

  • Uses

    For washing to decrease bacteria on skin.

  • Caution

    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 consult doctor if irritation and rash develops.

    Keep out of reach of children.

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

  • Directions

    • Wet bar with water.
    • Lather vigorously and wash skin.
    • Rinse and dry thoroughly.
  • Inactive Ingredients

    (Sodium Palmate and/or Sodium Tallowate, Sodium Cocoate and/or Sodium Palm Kernelate), Calcium Carbonate, Water, Glycerin, Sodium Chloride, Sodium Hydroxide, Fragrance,Tetrasodium EDTA, Tetrasodium Etidronate

  • PRINCIPAL DISPLAY PANEL - 144 Bar Case

    meridian®

    ITEM: UWA3
    DESCRIPTION: MERIDIAN® UNWRAPPED ANTIBACTERIAL DEODORANT SOAP #3
    SIZE: #3
    QUANTITY: 144 BARS / NET WT 2.6 OZ (75 g) PER BAR
    PO # _______
    CARTON # ________ OF _______
    MFG DATE: _______
    EXP DATE: ______
    MADE IN MALAYSIA

    MANUFACTURED EXCLUSIVELY FOR BOB BARKER COMPANY, INC.
    7925 PURFOY RD., FUQUAY VARINA, NC 27526

    BULK SHIPMENT NOT FOR RETAIL
    ITEM: UWA3
    SIZE: #3

    PRINCIPAL DISPLAY PANEL - 144 Bar Case
  • INGREDIENTS AND APPEARANCE
    MERIDIAN UNWRAPPED ANTIBACTERIAL DEODORANT 
    benzethonium chloride soap
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:53247-137
    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)  
    SODIUM TALLOWATE, BEEF (UNII: 07RIK6QMEW)  
    Sodium Cocoate (UNII: R1TQH25F4I)  
    Sodium Palm Kernelate (UNII: 6H91L1NXTW)  
    Calcium Carbonate (UNII: H0G9379FGK)  
    Water (UNII: 059QF0KO0R)  
    Glycerin (UNII: PDC6A3C0OX)  
    Sodium Chloride (UNII: 451W47IQ8X)  
    Sodium Hydroxide (UNII: 55X04QC32I)  
    EDETATE SODIUM (UNII: MP1J8420LU)  
    ETIDRONATE TETRASODIUM (UNII: CZZ9T1T1X4)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:53247-137-011000 in 1 CASE06/01/2017
    111 g in 1 APPLICATOR; Type 0: Not a Combination Product
    2NDC:53247-137-02500 in 1 CASE06/01/2017
    232 g in 1 APPLICATOR; Type 0: Not a Combination Product
    3NDC:53247-137-03144 in 1 CASE06/01/2017
    375 g in 1 APPLICATOR; Type 0: Not a Combination Product
    4NDC:53247-137-04200 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)
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