Rurina
FDA Label NDC 71867-0001

Full FDA labeling including Indications, Dosage, Usage, and Precautions

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Telom-x Gene Co., Ltd. for the product Rurina (NDC 71867-0001). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.

This specific version of the label includes detailed information regarding otc - active ingredient, inactive ingredient, otc - purpose, warnings, otc - keep out of reach of children, indications & usage, dosage & administration, package label.principal display panel, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

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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