Provtect Hand Sanitizer
FDA Label NDC 81754-010

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Ignal for the product Provtect Hand Sanitizer (NDC 81754-010). 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, inactive ingredient, purpose, warnings, keep out of reach of children, uses, directions, other information, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Active Ingredient

Chlorine Dioxide 0.01%

Inactive Ingredient

Water

Purpose

Antimicrobial

Warnings

For external use only. Avoid direct sunlight and store in a cool place.
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Do not use
• in children less than 2 months of age
• internal wound • inhalation by fumigation
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When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.
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Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.
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Keep out of reach of children. If nauseous feeling or sickness occurs, when swallowed, get medical help or contact a Poison Control Center right away.

Keep Out Of Reach Of Children

If nauseous feeling or sickness occurs, when swallowed, get medical help or contact a Poison Control Center right away.

Uses

■ Hand Sanitizer help to reduce germs and inactivate viruses that potentially can cause disease.

Directions

■ Spray on or Wet palms, rub hands thoroughly together until dry.
■ Supervise children under 6.

Other Information

■ Store between 5-20C (41-68F)
■ Avoid freezing and excessive heat above 40C (104F)

* Please review the disclaimer below.