Medilive
FDA Label NDC 78089-026

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Endeks Kimya Sanayi Ve Ticaret Anonim Sirketi for the product Medilive (NDC 78089-026). 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 drug facts, active ingredient, purpose, uses, warnings, directions, other information, packaging, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Drug Facts

Active Ingredient

Ethyl Alcohol 70%

Purpose

Antiseptic

Uses

• Hand Sanitizer to decrease bacteria on the skin • Recommended for repeated use • For use when soap and water are not available

Warnings

For external use only. Flammable, keep away from fire or flame.

Do not use

  • on open skin wounds
  • in children less than 2 months of age.

    • Stop use and ask a doctor if

    • irritation and redness develop
    • condition persists for more than 72 hours

Directions

  • Wet hands thoroughly with product and allow to dry without wiping
  • Supervise children under 6 years of age when using this product to avoid swallowing

Other Information

  • Do not store in direct sunlight
  • Store below 50°C / 105°F
  • Avoid freezing and excessive heat above 40°C (104°F)

Packaging

Image (Label1)

Image (Label1)

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