Label: ALCOHOL FREE SANITIZING 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 July 26, 2020

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  • Active Ingredients

    Benzalkonium chloride 0.1%

  • Purpose

    Antiseptic

  • Uses

    Antiseptic (skin) cleanser.For personal hand hygiene to help

    prevent the spread of bacteria.

  • WARNINGS

    For external use, do not inhale or ingest. Keep out of reach of children.
    Avoid contact with broken skin and keep out of eyes. In case of contact with eyes, flush thoroughly with water.
    Store below 43℃. Avoid lights and preserve in cool, dry and ventilated places.
    Please test on a small area of skin before use, and stop use if skin irritation develops.
    Shall not apply as sanitizing for metalware.

  • DO NOT USE

    /

  • WHEN USING

    /

  • STOP USE

    /

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children.
    Avoid contact with broken skin and keep out of eyes. In case of contact with eyes, flush thoroughly with water.

  • Directions

    Adults and children over 2 years.For occasional and personal domestic use.Supervise children when they use this product.
    Spray it on your hands and rub thoroughly for at least 30 seconds. Allow to dry.

  • STORAGE AND HANDLING

    Store below 43℃. Avoid lights and preserve in cool, dry and ventilated places.
    Please test on a small area of skin before use, and stop use if skin irritation develops.
    Shall not apply as sanitizing for metalware.

  • INACTIVE INGREDIENT

    AQUA, PEG-40 HYDROGENATED CASTOR OIL,PARFUM, ALOE BARBADENSIS LEAF EXTRACT, CAMELLIA SINENSIS EXTRACT, ROSMARINUS OFFICINALIS (ROSEMARY) LEAF EXTRACT, TOCOPHEROL.

  • Label

    2

  • INGREDIENTS AND APPEARANCE
    ALCOHOL FREE SANITIZING 
    alcohol free sanitizing spray
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:74743-003
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE0.1 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F)  
    METHYL BENZOATE (UNII: 6618K1VJ9T)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    CAMELLIA SINENSIS WHOLE (UNII: C5M4585ZBZ)  
    ROSEMARY (UNII: IJ67X351P9)  
    TOCOPHEROL (UNII: R0ZB2556P8)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:74743-003-01100 g in 1 BOTTLE; Type 0: Not a Combination Product04/08/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A04/08/2020
    Labeler - Guangzhou Joy Claire Biological Technology Co., Ltd (418209894)
    Registrant - Guangzhou Joy Claire Biological Technology Co., Ltd (418209894)
    Establishment
    NameAddressID/FEIBusiness Operations
    Guangzhou Joy Claire Biological Technology Co., Ltd418209894manufacture(74743-003)
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