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

DISCLAIMER: Most OTC drugs are not reviewed and approved by 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 March 15, 2023

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  • Drug Facts


  • ACTIVE INGREDIENT:

    Alcohol, 62%

  • Purpose

    Antiseptic

  • USE

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

  • WARNING:

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

  • When using this product

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

  • Ask a doctor before use if you have

    • deep wounds, animals bites or serious burns.

  • Stop use and ask a doctor if

    • condition persists.

  • Keep out of reach of children.

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

  • DIRECTIONS:

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

  • INACTIVE INGREDIENTS

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

  • REF: P779114 NDC 43128-114-03

    Made in China
    www.ProAdvantagebyNDC.com

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

  • PRINCIPAL DISPLAY PANEL

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

  • Product Labels

    Hand Sanitizer Label

  • INGREDIENTS AND APPEARANCE
    PRO ADVANTAGE INSTANT HAND SANITIZER 
    alcohol liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:43128-114
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL620 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    DMDM HYDANTOIN (UNII: BYR0546TOW)  
    Product Characteristics
    Color    Score    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:43128-114-031 in 1 PACKAGE03/08/2013
    1118 mL in 1 BOTTLE; Type 0: Not a Combination Product
    Image of Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333E03/08/2013
    Labeler - NDC National Distribution & Contracting, Inc. (009831413)
    Establishment
    NameAddressID/FEIBusiness Operations
    Dukal088520668manufacture(43128-114)
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