Label: RURINA- sulfate, potassium ion, chloride ion liquid

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

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Drug Label Information

Updated November 7, 2017

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  • ACTIVE INGREDIENT

    Sulfate, Potassium Ion, Chloride Ion

  • INACTIVE INGREDIENT

    Al, Ca, Ga, La, Li, Mn, Nd, Si, Zn

  • PURPOSE

    First aid to help prevent infection in minor:

    • cuts
    • scrapes
    • burns

  • WARNINGS

    Do not use

    • if you are allergic to any of the ingredients
    • in the eyes
    • over large areas of the body

    Ask a doctor before use if you have

    • deep or puncture wounds
    • animal bites
    • serious burns

    Stop use and ask a doctor if

    • you need to use longer than 1 week
    • condition persists or gets worse
    • rash or other allergic reaction develops
  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children.

  • INDICATIONS & USAGE

    Apply to the area which is wounded or burnt

  • DOSAGE & ADMINISTRATION

    for external use only

  • PRINCIPAL DISPLAY PANEL

    label

  • INGREDIENTS AND APPEARANCE
    RURINA 
    sulfate, potassium ion, chloride ion liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71867-0001
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SULFATE ION (UNII: 7IS9N8KPMG) (SULFATE ION - UNII:7IS9N8KPMG) SULFATE ION3.6 g  in 1 L
    POTASSIUM CATION (UNII: 295O53K152) (POTASSIUM CATION - UNII:295O53K152) POTASSIUM CATION0.25 g  in 1 L
    CHLORIDE ION (UNII: Q32ZN48698) (CHLORIDE ION - UNII:Q32ZN48698) CHLORIDE ION0.11 g  in 1 L
    Inactive Ingredients
    Ingredient NameStrength
    MAGNESIUM (UNII: I38ZP9992A)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:71867-0001-11 L in 1 BOTTLE, GLASS; Type 0: Not a Combination Product07/01/2017
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other07/01/2017
    Labeler - TELOM-X GENE Co., Ltd. (694948208)
    Registrant - TELOM-X GENE Co., Ltd. (694948208)
    Establishment
    NameAddressID/FEIBusiness Operations
    TELOM-X GENE Co., Ltd.694948208manufacture(71867-0001)
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