Label: MIMO ANTI-BACTERIAL OATS-AVENA- 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 develops.

  • 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, Water, Sodium Palm Kernelate, Calcium Carbonate, Glycerin, Zea Mays (Corn) Starch, Avena Sativa (Oat) Bran, Sodium Chloride, Fragrance, Etidronic Acid, Tetrasodium EDTA, Titanium Dioxide, D&C Orange No. 4, D&C Yellow No. 10.

  • SPL UNCLASSIFIED SECTION

    MIMO OATS bar is your best alternative to moisturize your skin and protect it from germs. The formula includes oils that are 100% vegetable-derived along with other ingredients to make your skin feel soft, clean, and fresh.

    Distributed by: C7 Global LLC

    San Juan, PR 00922

    Tel: 787-710-7345

    Email: info@c7global.com

    Web: www.c7global.com

    Made in Columbia

  • PRINCIPAL DISPLAY PANEL

    MIMO HYDRATE SKIN

    OATS - AVENA

    ANTIBACTERIAL MOISTURIZER

    EXFOLIATES SKIN

    3 BARS

    3-3.2 OZ SOAP BARS (90g)

    NET WT 9.6 oz OZ (270g)

    label

  • INGREDIENTS AND APPEARANCE
    MIMO ANTI-BACTERIAL OATS-AVENA 
    benzalkonium chloride soap
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:70841-0470
    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
    EDETATE SODIUM TETRAHYDRATE (UNII: L13NHD21X6)  
    D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)  
    SODIUM PALMATE (UNII: S0A6004K3Z)  
    WATER (UNII: 059QF0KO0R)  
    CALCIUM CARBONATE (UNII: H0G9379FGK)  
    SODIUM PALM KERNELATE (UNII: 6H91L1NXTW)  
    STARCH, CORN (UNII: O8232NY3SJ)  
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    ETIDRONIC ACID (UNII: M2F465ROXU)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    OAT BRAN (UNII: KQX236OK4U)  
    D&C ORANGE NO. 4 (UNII: Q1LIY3BO0U)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:70841-0470-33 in 1 BOX07/23/201805/10/2024
    190 g in 1 PACKAGE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)07/23/201805/10/2024
    Labeler - C7 Global LLC (831519728)
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