Label: QUICK N CLEAN ANTISEPTIC HAND WIPE - benzalkonium chloride swab 

  • Label RSS
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph final

NOTE: Most over the counter (OTC) are not reviewed and approved by the FDA. However, they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Drug Label Information

Updated 06/10

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  • PRINCIPAL DISPLAY PANEL

    Quick n Clean Antiseptic Hand Wipe

    Contains 1 Single Use Wipe

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  • Drug Facts

    Active Ingredient

    Benzalkonium Chloride, 0.133% w/v

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  • PURPOSE

    Purpose

    First Aid Antiseptic

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  • WHEN USING

    USE: Antiseptic Cleansing of face, hands and body without soap and water, Air dries in seconds.

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  • DO NOT USE

    DO NOT USE: in the eyes or apply over larger area of the body.

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  • STOP USE

    STOP USE: if irritation, redness or other symptoms develop. Consult a doctor if the condition persists or gets worse.

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  • KEEP OUT OF REACH OF CHILDREN

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

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  • INDICATIONS & USAGE

    DIRECTIONS: Tear open packet, unfold and use as a washcloth.

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  • INACTIVE INGREDIENT

    INACTIVE INGREDIENTS: Distilled Water

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  • PRINCIPAL DISPLAY PANEL

    Distributed By:

    Total Resources International

    Walnut, CA 91789

    www.totalresourcesintl.com

    Made in China

    REORDER NO: 00-TOW-94185

    NDC 65517-0016-1

    Hand Wipe Label

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  • INGREDIENTS AND APPEARANCE
    QUICK N CLEAN ANTISEPTIC HAND WIPE 
    benzalkonium chloride swab
    Product Information
    Product Type HUMAN OTC DRUG LABEL Item Code (Source) NDC:65517-0016
    Route of Administration TOPICAL DEA Schedule     
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    BENZALKONIUM CHLORIDE (BENZALKONIUM) BENZALKONIUM CHLORIDE 0.00186 mL  in 1.4 mL
    Inactive Ingredients
    Ingredient Name Strength
    WATER  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:65517-0016-1 1.4 mL in 1 POUCH
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC monograph final part333 06/01/2010
    Labeler - Dukal Corporation (791014871)
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