Virx
FDA Label NDC 40104-703

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Ningbo Pulisi Daily Chemical Products Co., Ltd for the product Virx (NDC 40104-703). 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 warnings, inactive ingredient, otc - active ingredient, otc - keep out of reach of children, otc - purpose, package label.principal display panel, otc - stop use, indications & usage, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Warnings

  • For external use only * Flammable * Keep away from fire or flame
  • Do not store above 40 degrees Celcius (105 degrees Fahrenheit)
  • Do not use in mouth, ears and eyes
  • When using this product, avoid contact with eyes
  • In case of contact, flush eyes with water

Inactive Ingredient

Deionized Water, Glycerin, Isopropyl Myristate, Propylene Glycol, Tocopheryl Acetate, Aminomethyl Propanol, Carbomer, Fragrance.

Otc - Active Ingredient

Ethyl Alcohol 62%......................................................................................Antiseptic

Otc - Keep Out Of Reach Of Children

Keep out of reach of children. Children must be supervised when using this product.

Otc - Purpose

Uses Hand Sanitizer to help decrease bacteria on the skin.

Package Label.Principal Display Panel

MM1

Otc - Stop Use

Stop use and seek a doctor if redness or irritation develops and persists for more than 72 hours.

Indications & Usage

Directions:
  • Pump as needed into your palms and thoroughly spread on both hands
  • Rub into skin until dry

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