Cloravir Hand Sanitizer
FDA Label NDC 71544-0010

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by My Corp.,ltd for the product Cloravir Hand Sanitizer (NDC 71544-0010). 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, inactive ingredient, otc - purpose, otc - keep out of reach of children, indications & usage, warnings, dosage & administration, package label.principal display panel, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Otc - Active Ingredient

titanium dioxide, hypochlorous acid

Inactive Ingredient

Coumarin, Linalool, Quercetin, Water

Otc - Purpose

  • Do not dilute spray
  • Use at strength for maximum effectiveness
  • Spray directly, from a distance of about 8 to 10 inches. For equipment or products that are difficult to spray, apply liquid to clean gauze or cotton swab.

Otc - Keep Out Of Reach Of Children

keep out of reach of the children

Indications & Usage

  • Wipe with gauze or cotton swab and let air dry. Spray clothes, equipment, and indoor objects for sterilization and deodorization as required.

Warnings

For external use only. 

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

Stop use and ask a doctor if irritation or rash occurs develop and persist for more than 72 hours.

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

Package Label.Principal Display Panel

Label (Label)

Label (Label)

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