Virx
FDA Label NDC 29860-200

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 United Group Co., Ltd. for the product Virx (NDC 29860-200). 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, warnings, otc - purpose, otc - when using, otc - stop use, otc - keep out of reach of children, indications & usage, inactive ingredient, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Otc - Active Ingredient

Ethyl Alcohol 62.0%..................................Antimicrobial

Warnings

For external Use only. Flammable. Keep away from heat and flame.

Otc - Purpose

Use hand sanitizer to help reduce bacteria on the skin that may cause disease.

Otc - When Using

When using this product avoid contact with face, eyes and broken skin.  In case of eye contact, flush with plenty of water and seek medical advice.

Otc - Stop Use

Stop use and ask a doctor if irritation or redness develops.

Otc - Keep Out Of Reach Of Children

Keep out of the reach of children.  If swallowed, get medical help or contact a Poison Control Center.

Indications & Usage

Directions wet hands thoroughly with product and rub into skin until dry. Children under 6 years of age should be supervised by an adult when using this product.

Inactive Ingredient

Water (Agua), Triethanolamine, Carbomer, Aloe Barbadensis (Aloe Vera) Gel, Fragrance, Glycerin, Propylene Glycol and Tocopheryl Acetate (Vitamin E).

Package Label.Principal Display Panel

MM1

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