Purox Hand Sanitizer
FDA Label NDC 78186-001

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Purox for the product Purox Hand Sanitizer (NDC 78186-001). 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, purpose, use, warnings, otc - when using, otc - stop use, otc - keep out of reach of children, do not use, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Active Ingredient

Alcohol 85% v/v

Purpose

Antimicrobial

Use

Hand Sanitizer to help reduce bacteria on the skin.

Warnings

Flammable. Keep away from heat or flame

For external use only

Otc - When Using

When using this product

  • do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water.

Otc - Stop Use

Stop use and ask a doctor if

  • irritation or rash appears and lasts.

Otc - Keep Out Of Reach Of Children

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

Do Not Use

  • in children less than 2 months of age
  • on open skin wounds

Directions

  • Place enough product in your palm to thoroughly spread on both hands and rub into th skin until dry.
  • Children under 6 years old should be supervised when using this product.

Other Information:

  • store between 106F (41C)
  • may discolor certain fabrics or surfaces

Inactive Ingredients:

Deionized Water, Aloe, Triethanolamine, Carbomer

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