Label: YAN PLUS SUPER MEDIC- colloidal silver spray

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

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Drug Label Information

Updated May 9, 2020

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  • ACTIVE INGREDIENT

    Active ingredients
    COLLOIDAL SILVER 0.002%

  • INACTIVE INGREDIENT

    Inactive ingredients
    Water(Alkaline), Potassium chloride, Sodium Silicate

  • PURPOSE

    Purpose: SANITIZER

  • WARNINGS

    Warnings

    For external use only. Do not spray in or near eyes.
    Stop use and ask doctor if as adverse reaction occurs or persists.
    --------------------------------------------------------------------------------------------------------
    Do not use
    • in children less than 2 months of age: ask a doctor.
    • on open skin wounds
    --------------------------------------------------------------------------------------------------------
    Indications
    .Surface of the skin and general objects for disinfection.
    --------------------------------------------------------------------------------------------------------
    When using this product
    Keep out of the reach of children. If swallowed, get medical help or contact a Poison Control immediately.

  • KEEP OUT OF REACH OF CHILDREN

    If swallowed, get medical help or contact a Poison Control immediately.

  • Uses

    Uses
    Yan Plus Super Medic Sanitizer kills 99.9% of germ on contact and are more powerful than alcohol based sanitizers.
    YAN Pus Super Medic is thoroughly Lab tested to ensure the safety

  • Directions

    Directions
    • Spray this evenly on the surface of the skin or the object, or rub it on the surface 2times. Will dry out soon.

  • Other information

    Other information
    • No animals were used to test this product.
    • Recommend for repeated use.

  • QUESTIONS

    Questions
    www.tripeople.co.kr
    TEL: 82-70-4350-1760

  • PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

    Image of bottle

  • INGREDIENTS AND APPEARANCE
    YAN PLUS SUPER MEDIC 
    colloidal silver spray
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:76642-010
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SILVER (UNII: 3M4G523W1G) (SILVER - UNII:3M4G523W1G) SILVER0.004 g  in 200 mL
    Inactive Ingredients
    Ingredient NameStrength
    Water (UNII: 059QF0KO0R)  
    Potassium chloride (UNII: 660YQ98I10)  
    SODIUM SILICATE (UNII: IJF18F77L3)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:76642-010-01200 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product05/01/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other05/01/2020
    Labeler - TRIPEOPLE COSMETIC CO.,LTD. (695004869)
    Registrant - TRIPEOPLE COSMETIC CO.,LTD. (695004869)
    Establishment
    NameAddressID/FEIBusiness Operations
    TRIPEOPLE COSMETIC CO.,LTD.695004869manufacture(76642-010)
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