Purifi Hand Sanitizer Solution
FDA Label NDC 80659-301

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Purifi Llc for the product Purifi Hand Sanitizer (NDC 80659-301). 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 other, otc - active ingredient, otc - purpose, indications & usage, warnings, otc - when using, otc - stop use, otc - keep out of reach of children, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Other

Drug Facts

Otc - Active Ingredient

Active ingredient

Benzalkonium Chloride 0.13%

Otc - Purpose

Purpose

Antimicrobial

Indications & Usage

Uses

Hand sanitizing to help reduce bacteria on the skin

Warnings

Warnings

For external use only.

Otc - When Using

When using this product avoid contact with the eyes. In case of contact, rinse eyes thoroughly with water.

Otc - Stop Use

​Stop use and ask a doctor if irritation or redness 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 immediately.

Dosage & Administration

Directions

Apply liberally to hands and gently rub until dry. Reapply every 6 hours.

Inactive Ingredient

Inactive ingredients

purified water, glycerin, aloe barbadensis leaf juice

* Please review the disclaimer below.