Label: SHOPRITE LIQUID HAND SANITIZER- alcohol liquid

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated November 13, 2023

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  • Drug Facts

  • Active ingredient[s]

    Alcohol 80% v/v

    Purpose

    Antiseptic

  • Use[s]

    Hand sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.

  • Warnings

    For external use only. Flammable. Keep away from heat or flame.

    Do not use

    • on children less than 2 months of age
    • on open skin wounds

    When using this product

    keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.

    Stop use and ask a doctor if 

    irritation or rash occurs. These may be signs of  a serious condition.

    Keep out of reach of children.

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

  • Directions

    • Place enough product on hands to cover all surfaces. Rub hands together until dry.
    • Superivse children under 6 years of age when using this product to avoid swallowing.
  • Other information

    • Store between 59-86°F (15-30°C)
    • Avoid freezing and excessive heat above 104°F (40°C)
  • Inactive ingredients

    glycerin, hydrogen peroxide, purified water USP

  • Questions or comments?

    1-844-308-8600

  • Package Labeling:

    Label6

  • INGREDIENTS AND APPEARANCE
    SHOPRITE LIQUID HAND SANITIZER 
    alcohol liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:41190-326
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL80 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX)  
    HYDROGEN PEROXIDE (UNII: BBX060AN9V)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:41190-326-00236 mL in 1 BOTTLE; Type 0: Not a Combination Product01/30/202112/01/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00301/30/202112/01/2024
    Labeler - Wakefern Food Corp (069722418)
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