Label: HAND SANITIZER- hand sanitizer spray spray

  • 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 January 6, 2021

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  • Active Ingredient

    Ethyl Alcohol 75%

  • Purpose

    Antimicrobial

  • Uses

    Use: Hand sanitizer to help, reduce bacteria on skin

  • Warnings

    Warnings. Flammable. Keep away from fire or flame For extend use or When using this product do not use in or near the eyes. in case of contact, rinse eyes thoroughly with water. stop use and ask a doctor if imitation or rash appears and lasts. Keep out of reach of children. I swallowed, get medical help or contact a Poison Control Center immediately

  • DO NOT USE

    When using this product do not use in or near the eyes

  • WHEN USING THIS PRODUCT

    When using this product do not use in or near the eyes.

  • STOP USE

    stop use and ask a doctor if imitation or rash appears and lasts.

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center immediately

  • Directions

    Directions: Put enough product n your palm to cover hands and rub hands together brady until dry

    Children 6 years of age should be supervised when using

  • Other information

    Other information: Store at room temperature

    Keep container tightly closed in a dry and well-ventilated place

    Avoid storage under direct sunlight

    Keep out of reach of children

  • Inactive ingredients

    Inactive ingredients: Water (Aqua), Isopropyl Alcohol , Aloe Barbadensis Leaf Juice,

    Caprylyl Glycol, Glycerin, Isopropyl Miristate, Acrylates/C10-30 Alky Acrylate Cross polymer,

    Aminomethyl Propanol, Fragrance(Parfum)

  • Package Label - Principal Display Panel

    74881-005-01 150ml 1

    74881-005-02 150ml

    74881-005-02 150ml

  • INGREDIENTS AND APPEARANCE
    HAND SANITIZER 
    hand sanitizer spray spray
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:74881-005
    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
    CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
    ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    CARBOMER INTERPOLYMER TYPE A (55000 CPS) (UNII: 59TL3WG5CO)  
    WATER (UNII: 059QF0KO0R)  
    ISOPROPYL ALCOHOL (UNII: ND2M416302)  
    1-AMINOBUTAN-2-OL (UNII: 19453GN3YQ)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:74881-005-01150 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product06/23/2020
    2NDC:74881-005-02150 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product06/23/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A06/23/2020
    Labeler - Huizhou Baozi Biotechnology Co., Ltd. (419304583)
    Registrant - Huizhou Baozi Biotechnology Co., Ltd. (419304583)
    Establishment
    NameAddressID/FEIBusiness Operations
    Huizhou Baozi Biotechnology Co., Ltd.419304583manufacture(74881-005)
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