Label: ANTIBACTERIAL HAND SANITIZER- hand sanitizer liquid

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved drug other

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Drug Label Information

Updated March 29, 2020

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  • ACTIVE INGREDIENT

    P-chloro-m-dimethylphenol

  • DOSAGE & ADMINISTRATION

    store in a cool, dry, dark place.

  • KEEP OUT OF REACH OF CHILDREN

    keep out of reach of children.

  • WARNINGS

    This product is hand sanitizer for external use.

    Do not take it orally. In case of contact with eyes, use plenty of water immediately.

  • INDICATIONS & USAGE

    Rotate the pump head to the front exit, gently press the pump head, press out an appropriate amount of foam on both hands, and fully rub about 2 minutes, then wash with clean water.

  • PURPOSE

    Disinfection
    Sterilization
    No Rinseing

  • INACTIVE INGREDIENT

    GLYCERIN
    COCAMDOPROPYL BETAINE
    COCAMINE
    MAGNESIUM CHLORIDE
    METMCHL OITHIAOINONE
    SODIUM CHLORIDE
    PROPYLENE GLYCOL
    METHYUSOTHIAZOLINONE
    EDETIC ACID
    SODIUM LAURETH-5 SULFFATE
    WATER

  • PRINCIPAL DISPLAY PANEL

    label

  • INGREDIENTS AND APPEARANCE
    ANTIBACTERIAL HAND SANITIZER 
    hand sanitizer liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:54607-003
    Route of AdministrationEXTRACORPOREAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    2-CHLORO-4,5-DIMETHYLPHENOL (UNII: 601F79M480) (2-CHLORO-4,5-DIMETHYLPHENOL - UNII:601F79M480) 2-CHLORO-4,5-DIMETHYLPHENOL1.5 mg  in 500 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM LAURETH-5 SULFATE (UNII: 410Q7WN1BX)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)  
    COCAMINE (UNII: 6724Q5747W)  
    WATER (UNII: 059QF0KO0R)  
    METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)  
    EDETIC ACID (UNII: 9G34HU7RV0)  
    MAGNESIUM CHLORIDE (UNII: 02F3473H9O)  
    Product Characteristics
    Color    Score    
    ShapeSize
    FlavorImprint Code suayi
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:54607-003-01500 mL in 1 BOTTLE; Type 0: Not a Combination Product03/29/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other03/29/2020
    Labeler - Wuxi Yongning Daily Chemical Factory (546074675)
    Establishment
    NameAddressID/FEIBusiness Operations
    Wuxi Yongning Daily Chemical Factory546074675manufacture(54607-003)
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