Vunnex Hand Sanitizer
FDA Label NDC 79450-001

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Vunnex International Llc for the product Vunnex Hand Sanitizer (NDC 79450-001). 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 active ingredient, purpose, warnings, keep out of reach of children., uses, directions, other information, inactive ingredients, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Active Ingredient

Alcohol 80% v/v

Purpose

Antiseptic.

Warnings

For external use only. Flammable. Keep away from heat or flame.

Do not use• In children less than 2 months of age
• On open skin wounds

 When using this product keep out of eyes, ears, and mouth. In case of contact  rinse eyes  thoroughly with water.

 Stop use and ask a doctor

  • if irritation or rash occurs. 
  • These may be signs of a serious condition.

Keep Out Of Reach Of Children.

If swallowed, get medical help or contact a Poison Control Center right away.

Uses

Hand Sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.

Directions

  • Place enough product on hands to cover all surfaces. Rub hands together until dry.
  • Supervise children under 6 years of age when using this product to avoid swallowing.

Other Information

  • Store between 15-30C (59-86F)
  • Avoid freezing and excessive heat above 40C (104F)

Inactive Ingredients

GLYCERIN,HYDROGEN PEROXIDE,WATER

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