Virx
FDA Label NDC 50438-807

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Filo America for the product Virx (NDC 50438-807). 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, otc - purpose, warnings, otc - when using, otc - stop use, otc - keep out of reach of children, warnings and precautions, 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

Active Ingredient...........................................................PurposeEthyl Alcohol 62%...........................................................................Antiseptic

Otc - Purpose

Use to decrease bacteria on the skin.

Warnings

WarningsFor external use only * Flammable * Keep away from fire or flame.

Otc - When Using

When using this product avoid contact with mouth, ears, and eyes.  In case of contact, flush eyes with water.
DirectionsPump into palms and thoroughly rub into skin until dry.

Otc - Stop Use

Stop use and ask a doctor if redness or irritation develops and lasts more than 72 hours.

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 right away.

Warnings And Precautions

Other Information * store at 20 degrees Celcius (68 degrees to 77 degrees Farenheit) * may discolor fabrics.

Inactive Ingredient

Deionized water, glycerin, isopropyl myristate, propylene glycol, tocopheryl acetate, aminomethyl propanol, carbomer, fragrance and yellow 5.

Package Label.Principal Display Panel

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