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  5. Label Information: Rurina

FDA Label for Rurina

View Indications, Usage & Precautions

Table of Contents

    1. OTC - ACTIVE INGREDIENT
    2. INACTIVE INGREDIENT
    3. OTC - PURPOSE
    4. WARNINGS
    5. OTC - KEEP OUT OF REACH OF CHILDREN
    6. INDICATIONS & USAGE
    7. DOSAGE & ADMINISTRATION
    8. PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Rurina Product Label

The following document was submitted to the FDA by the labeler of this product Telom-x Gene Co., Ltd.. The document includes published materials associated whith this product with the essential scientific information about this product as well as other prescribing information. Product labels may durg indications and usage, generic names, contraindications, active ingredients, strength dosage, routes of administration, appearance, warnings, inactive ingredients, etc.

Otc - Active Ingredient



Sulfate, Potassium Ion, Chloride Ion


Inactive Ingredient



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


Otc - 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

Otc - 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


Package Label.Principal Display Panel



label - label

label - label


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