Label: WEIS SIMPLY GREAT ADVANCED HAND SANITIZER WITH VITAMINS E AND B5- ethanol gel

  • NDC Code(s): 72956-100-02, 72956-100-08, 72956-100-16, 72956-100-28, view more
    72956-100-32
  • Packager: Weis Markets, Inc.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph not final

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 February 2, 2023

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  • Drug Facts

  • Active Ingredient

    Ethanol 75%

  • Purpose

    Antiseptic

  • Uses

    • Hand sanitizer to decrease bacteria on skin • Recommended for repeated use

  • Warnings

    • For external use only

    Flammable. Keep away from fire or flame.

    When using this product avoid contact with face, eyes and broken skin. If eye contact occurs, flush thoroughly with water and seek medical advice.

    Stop use and ask doctor if irritation and redness develops.

    Keep out of reach of children.

  • Directions

    • Wet hands thoroughly with product and rub into skin until dry. • Children under 6 years of age should be supervised by an adult when using this product.

  • Inactive Ingredients:

    Water (Aqua), Polysorbate 20, Glycerin, Tocopheryl Acetate, Panthenol, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Aminomethyl Propanol, Fragrance (Parfum).

  • SPL UNCLASSIFIED SECTION

    KILLS GERMS

    HELPS REDUCE THE RISK OF INFECTIONS

    COMPARE TO PURELL® ADVANCED HAND SANITIZER*

    *PURELL® ADVANCED HAND SANITIZER IS A REGISTERED TRADEMARK OF GOJO INDUSTRIES, INC. DISCLAIMER

    PACKED FOR
    WEIS MARKETS, INC.
    SUNBURY, PA 17801
    www.weismarkets.com

    PRODUCT OF USA

    Our Weis Simply Great Products are Satisfaction Guaranteed or Your Money Back

  • Packaging

    Weis1

    Weis2

  • INGREDIENTS AND APPEARANCE
    WEIS SIMPLY GREAT ADVANCED HAND SANITIZER WITH VITAMINS E AND B5 
    ethanol gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:72956-100
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL75 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    POLYSORBATE 20 (UNII: 7T1F30V5YH)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    PANTHENOL (UNII: WV9CM0O67Z)  
    CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)  
    AMINOMETHYLPROPANOL (UNII: LU49E6626Q)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:72956-100-0259 mL in 1 BOTTLE; Type 0: Not a Combination Product01/01/2021
    2NDC:72956-100-08236 mL in 1 BOTTLE; Type 0: Not a Combination Product01/01/2021
    3NDC:72956-100-16473 mL in 1 BOTTLE; Type 0: Not a Combination Product01/01/2021
    4NDC:72956-100-32946 mL in 1 BOTTLE; Type 0: Not a Combination Product01/01/2021
    5NDC:72956-100-283785 mL in 1 BOTTLE; Type 0: Not a Combination Product01/01/2021
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A01/01/2021
    Labeler - Weis Markets, Inc. (007917420)
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