Label: NANO SILVER CLEANSER HAND SANITIZER- silver cation,alcohol spray

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

DISCLAIMER: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

Drug Label Information

Updated October 15, 2020

If you are a consumer or patient please visit this version.

  • Active ingredient

    SILVER CATION,ALCOHOL

  • USE

    Nano Silver Cleanser Hand sanitizer to help reduce bacteria that potentially can cause disease.

    For use when soap and water are not available.

    If you are new to the product, apply it on a small area and test

    to see if there is anything wrong with your skin

  • WHEN USING

    keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.

  • Warnings

    For external use only. Flammable. Keep away from heat or flame

    Don't put it on your face

    Hand sterilization and cleaning are possible, but they are

    not medicines

  • Do not use

    ● in children less than 2 months of age

    ● on open skin wounds

    Do not use in areas with abnormalities such as wound, eczema,

    and dermatitis

  • Stop use and ask doctor

    Stop use and ask doctor irritation or rash occurs. These may be signs of a serious condition.

    If you experience any of the following problems, do not use this product and contact your dermatologist, etc

    In case of abnormalities such as red spots, swelling,

    itching, irritation, etc. during use

  • PURPOSE

    Antimicrobial

  • Keep out of reach of children

    Keep out of reach of children

  • Direction

    ● Spray 2~3 time on the hand or general objects exposed to contamination and then dry with

    a tissue or dry cloth after 1 minute. Sprinkle 30cm below the face.

    ● Supervise children under 6 years of age when using this product to avoid swallowing

  • Other information

    ●Store between 15-30C (59-86F)

    ●Avoid freezing and excessive heat above 40C (104F)

    ●Year of manufacture:notation of separate diagram

    ●Expiration day:3years from manufacturing date

    ●Questions or Comments? please call 82-10-5327-9670

  • Inactive ingredients

    cypress oil, poiyoxyethylene sorbitan monolaurate, purified water

  • label

    79702-301-01 50ML

    79702-301-0179702-301-02 70ML

    79702-301-02

    79702-301-03 100ML

    79702-301-03

    79702-301-04 200ML

    79702-301-04

    79702-301-05 500ML

    79702-301-05

    79702-301-06 1000ML

    79702-301-06

  • INGREDIENTS AND APPEARANCE
    NANO SILVER CLEANSER HAND SANITIZER 
    silver cation,alcohol spray
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:79702-301
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SILVER CATION (UNII: 57N7B0K90A) (SILVER CATION - UNII:57N7B0K90A) SILVER CATION0.0025 g  in 100 mL
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL0.05 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    POLYSORBATE 20 (UNII: 7T1F30V5YH)  
    CUPRESSUS SEMPERVIRENS LEAF OIL (UNII: M7QUY89S4O)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:79702-301-0150 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product08/11/2020
    2NDC:79702-301-0270 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product08/11/2020
    3NDC:79702-301-03100 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product08/11/2020
    4NDC:79702-301-04200 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product08/11/2020
    5NDC:79702-301-05500 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product08/11/2020
    6NDC:79702-301-061000 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product08/11/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other08/11/2020
    Labeler - DDUnion, Co.,Ltd (694100331)
    Registrant - DDUnion, Co.,Ltd (694100331)
    Establishment
    NameAddressID/FEIBusiness Operations
    DDUnion, Co.,Ltd694100331manufacture(79702-301)