Puro Non-alcohol Foam Hand Sanitizer
FDA Label NDC 70415-405

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Cwgc La Inc. for the product Puro Non-alcohol Foam Hand Sanitizer (NDC 70415-405). 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, uses, warnings, otc - keep out of reach of children, otc - stop use, directions, inactive ingredients, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Active Ingredient

BENZALKONIUM CHLORIDE  0.13%

Purpose

Antibacterial

Uses

  • For handwashing to reduce bacteria on the skin. Recommended for repeated use.

Warnings

For external use only

Avoid contact with eyes. In case of eye contact, flush eyes with water.

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.

Otc - Stop Use

Stop use and ask a doctor if irritation or redness develops and persists.

Directions

  • Apply foam sanitizer to hands.
  • Rub over surfaces of both hands for 15 seconds.
  • No rinsing required.

Inactive Ingredients

Water, Coco-Glucoside, Laurtrimonium Chloride, Cocamidopropylamine Oxide, Citric Acid, Fragrance.

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