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

  • NDC Code(s): 71867-0001-1
  • Packager: TELOM-X GENE Co., Ltd.
  • 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 November 7, 2017

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

  • 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)