Label: PRO ADVANTAGE INSTANT HAND SANITIZER - alcohol liquid

  • NDC Code(s): 43128-114-03
  • Packager: NDC National Distribution & Contracting, Inc.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph not 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 03/13

If you are a consumer or patient please visit this version.

  • Drug Facts
  • ACTIVE INGREDIENT:

    Alcohol, 62%

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  • Purpose

    Antiseptic

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  • USE

    To help reduce bacteria on the hands that can potentially cause disease.

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  • WARNING:

    • For External Use Only
    • Flammable, Keep away from fire or flame.

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  • When using this product

    • Avoid contact with eyes, if this occurs rinse thoroughly with water and contact a physician.

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  • Ask a doctor before use if you have

    • deep wounds, animals bites or serious burns.

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  • Stop use and ask a doctor if

    • condition persists.

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  • Keep out of reach of children.

    • If swallowed get medical help or contact a Poison Control Center right away.

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  • DIRECTIONS:

    Apply a liberal amount to hands and rub hands thoroughly until dry. Do not rinse or wipe off gel.

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  • INACTIVE INGREDIENTS

    Water, Glycerin, Fragrance, Carbomer, Triethanolamine, DMDM Hydantoin

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  • REF: P779114 NDC 43128-114-03

    Made in China
    www.ProAdvantagebyNDC.com

    Manufactured for NDC, Inc.
    407 New Sanford Road, La Vergne, TN 37086

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  • PRINCIPAL DISPLAY PANEL

    Pro Advantage by NDC Instant
    Hand Sanitizer
    4 FL. OZ.
    ( 118 mL )
    Kills Germs With 62% Alcohol
    *+M220P77911480*

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  • Product Labels
  • INGREDIENTS AND APPEARANCE
    PRO ADVANTAGE INSTANT HAND SANITIZER  
    alcohol liquid
    Product Information
    Product Type HUMAN OTC DRUG LABEL Item Code (Source) NDC:43128-114
    Route of Administration TOPICAL DEA Schedule     
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    ALCOHOL (ALCOHOL) ALCOHOL 620 mg  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    WATER  
    GLYCERIN  
    TROLAMINE  
    DMDM HYDANTOIN  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:43128-114-03 1 in 1 PACKAGE
    1 118 mL in 1 BOTTLE
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC monograph not final part333E 03/08/2013
    Labeler - NDC National Distribution & Contracting, Inc. (009831413)
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