Label: NEXT 1 ANTI-BACTERIAL DEODORANT- benzalkonium chloride soap

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated January 1, 2024

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  • SPL UNCLASSIFIED SECTION

    Drug Facts

  • ACTIVE INGREDIENT

    Active ingredient

    Benzalkonium Chloride 0.1%

  • PURPOSE

    Purpose

    Antibacterial

  • INDICATIONS & USAGE

    Uses

    for washing to decrease bacteria on the skin

  • WARNINGS

    Warnings

    For external use only

  • WHEN USING

    When using this product do not use in or near the eyes, in case of eye contact, flush with water

  • STOP USE

    Stop use and ask a doctor if irritation or redness develop

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

  • DOSAGE & ADMINISTRATION

    Directions

    • Web bar with water.
    • Lather vigorously and wash skin.
    • Rinse and dry thoroughly.
  • INACTIVE INGREDIENT

    Inactive ingredients Sodium Palmate, Sodium Palm Kernelate, Water, Glycerin, Sodium Chloride, Sodium Lauryl Sulfate, Fragrance, Titanium Dioxide, Coconut Acid, Citric Acid, Etidronic Acid, Tetrasodium EDTA. May contain Caramel.

  • SPL UNCLASSIFIED SECTION

    Distributed by:

    Olivette Products, L.L.C.

    Bridgeton, MO 63044

    Phone: 1-800-325-8998

    MADE IN COLOMBIA

    • Kills germs
    • Odor protection

  • PRINCIPAL DISPLAY PANEL

    Next 1 TM

    Anti-bacterial

    Deodorant

    Bar Soap

    Contains no animal fat

    NET WT 5 OZ (142g)

    label

  • INGREDIENTS AND APPEARANCE
    NEXT 1 ANTI-BACTERIAL DEODORANT 
    benzalkonium chloride soap
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:51870-004
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE0.1 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM PALM KERNELATE (UNII: 6H91L1NXTW)  
    SODIUM LAURYL SULFATE (UNII: 368GB5141J)  
    EDETATE SODIUM (UNII: MP1J8420LU)  
    CARAMEL (UNII: T9D99G2B1R)  
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    COCONUT ACID (UNII: 40U37V505D)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    ETIDRONIC ACID (UNII: M2F465ROXU)  
    WATER (UNII: 059QF0KO0R)  
    SODIUM PALMATE (UNII: S0A6004K3Z)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:51870-004-05142 g in 1 BOX; Type 0: Not a Combination Product06/15/2017
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)06/15/2017
    Labeler - Keefe Group (839439601)
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