Label: NEXT1 ANTI-BACTERIAL DEODORANT SPORT- 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

    • Wet 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, Green 3, Red 33. 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

    Sport Bar

    Contains no animal fat

    NET WT 5 OZ (142g)

    label

  • INGREDIENTS AND APPEARANCE
    NEXT1 ANTI-BACTERIAL DEODORANT SPORT 
    benzalkonium chloride soap
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:51870-003
    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
    WATER (UNII: 059QF0KO0R)  
    SODIUM PALMATE (UNII: S0A6004K3Z)  
    SODIUM PALM KERNELATE (UNII: 6H91L1NXTW)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    CARAMEL (UNII: T9D99G2B1R)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM LAURYL SULFATE (UNII: 368GB5141J)  
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
    COCONUT ACID (UNII: 40U37V505D)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    ETIDRONIC ACID (UNII: M2F465ROXU)  
    EDETATE SODIUM (UNII: MP1J8420LU)  
    FD&C GREEN NO. 3 (UNII: 3P3ONR6O1S)  
    D&C RED NO. 33 (UNII: 9DBA0SBB0L)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:51870-003-05142 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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