Label: STAY SAFE HAND SANITIZER- alcohol solution

  • 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 June 9, 2020

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  • Drug Facts

  • Active ingredient

    Ethyl Alcohol 65%

  • Purpose

     Antiseptic

  • Use

    • Decreases bacteria on the hands
  • Warnings

    • For external use only.
    • Flammable. Do not use hear heat, fire or flame while smoking.

    Do not store where temperature exceeds 105℉.

    Do not get in eyes. In case of eye contact flush with water

    Do not inhale or ingest.

    Stop use and ask a doctor if skin irritation develops.

    Do not use on: Burns or open wounds.

    If swallowed, get medical help or contact poison control Center immediately.

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

  • Directions

    put small amount into palm of hands. Rub together until dry.

  • Inactive ingredients

    Water, glycerin, propyene glycol, carbomer, sodium hydroxide

  • Packaging

    image description

  • INGREDIENTS AND APPEARANCE
    STAY SAFE HAND SANITIZER 
    alcohol solution
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:74274-011
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL65 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:74274-011-0160 mL in 1 BOTTLE; Type 0: Not a Combination Product06/09/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333E06/09/2020
    Labeler - Huizhou Bliss Commodity Co., Ltd (417467331)
    Establishment
    NameAddressID/FEIBusiness Operations
    Huizhou Bliss Commodity Co., Ltd417467331manufacture(74274-011)
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