Label: NYC HEALTH HOSPITALS HAND SANITIZER- ethyl alcohol gel

  • 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 24, 2021

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  • Active Ingredients

    Ethyl Alcohol 75%v/v.

    Purpose: Antimicrobial

  • Purpose

    Antimicrobial

  • Uses

    • helps reduce bacteria on the skin that could cause disease
    • Recommended for repeated use
  • Warnings

    For external use only.

    Flammable. Keep away from fire or flame.

  • Safety Instructions

    Flammable, Keep away from fire and flame

  • Ask Doctor

    Stop Use and Ask a doctor if irritation or redness develops

  • KEEP OUT OF REACH OF CHILDREN

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

  • Other Information

    Store below 110°F (43°C)
    May discolor certain fabrics or surfaces.

  • Directions

    • Place enough product in your palm to thoroughly cover your hands
    • Rub hands together briskly until dry
    • Children under 6 years of age should be supervised when using this product.
  • Inactive Ingredients

    water, isopropyl alcohol, glycerin, carbomer copolymer, aminomethyl propanol, fragrance, propylene glycol, isopropyl myristate, propylene glycol, Aloe, Tocopheryl Acetate. Please review Label for further details

  • PRINCIPAL DISPLAY PANEL

    1

  • INGREDIENTS AND APPEARANCE
    NYC HEALTH HOSPITALS  HAND SANITIZER
    ethyl alcohol gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:50157-340
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL0.75 mL  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    ISOPROPYL ALCOHOL (UNII: ND2M416302)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    DENATONIUM BENZOATE (UNII: 4YK5Z54AT2)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)  
    .ALPHA.-TOCOPHEROL ACETATE, D- (UNII: A7E6112E4N)  
    AMINOMETHYLPROPANOL (UNII: LU49E6626Q)  
    CARBOMER COPOLYMER TYPE A (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 71DD5V995L)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:50157-340-6060 mL in 1 BOTTLE; Type 0: Not a Combination Product02/24/2021
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333E02/24/2021
    Labeler - Brands International (243748238)
    Registrant - Brands International (243748238)
    Establishment
    NameAddressID/FEIBusiness Operations
    Brands International243748238manufacture(50157-340)
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