Label: ANCOS SILVER ION HAND SANITIZER gel

  • 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 August 24, 2020

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  • Main Active Ingredients and Content

    Silver ion: 0.01%, Ethyl alcohol: 62%(v/v)

  • Purpose

    Antibacterial

  • Uses

    The product has antibacterial effect on E coli, Staphylococcus aureus and Candida albicans, and can be used for hand disinfection in places such as intensive care unit, outpatient service, emergency room, ward and clinics, as well as in environment such as home and social places, especially when water is not available

  • Directions

    Hand hygiene and disinfection: Take an appropriate amount of disinfectant to the palm, rub according to the hand disinfection code instructions, ensure that the sanitizer completely covers the skin of the hand sand wait for one minute until dry

  • Warning

    • Sanitizer for external use, shall not betaken orally and shall be placed out of children's reach.
    • Avoid using with antagonist drugs
    • Those with allergies shall use
  • Other Tips

    Protect from light and store airtight at room temperature

  • Precautions

    Do not use this product in or near the eyes In case of contact, rinse eyes If irritation or rash appears and persists, stop using and consult the doctor.Please place out of children's reach. If swallowed, seek medical help or contact a Poison Control Center immediately

  • other ingredients

    Purified water, Glycerol, Carbomer, Menthol

  • WHEN USING

  • STOP USE

  • KEEP OUT OF REACH OF CHILDREN

  • Package Label - Principal Display Panel

    75139-006-02 500ml100ml

  • INGREDIENTS AND APPEARANCE
    ANCOS SILVER ION HAND SANITIZER 
    ancos silver ion hand sanitizer gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:75139-006
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SILVER CATION (UNII: 57N7B0K90A) (SILVER CATION - UNII:57N7B0K90A) SILVER CATION0.01 g  in 100 mL
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL62 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX)  
    MENTHOL (UNII: L7T10EIP3A)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:75139-006-01100 mL in 1 BOTTLE; Type 0: Not a Combination Product04/28/2020
    2NDC:75139-006-02500 mL in 1 BOTTLE; Type 0: Not a Combination Product04/28/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A04/28/2020
    Labeler - Anson Bio-Technology Co., Ltd. (547087171)
    Establishment
    NameAddressID/FEIBusiness Operations
    Anson Bio-Technology Co., Ltd.547087171manufacture(75139-006)
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