U Hand Sanitizer Classic Solution
FDA Label NDC 72119-004

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Blue Sea Aerosol & Daily Care Co., Ltd for the product U Hand Sanitizer Classic (NDC 72119-004). 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(s), purpose, use, warnings, otc - when using, otc - stop use, otc - keep out of reach of children, directions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Active Ingredient(S)

Benzalkonium Chloride 0.13%

Purpose

Antiseptic

Use

For Hand Sanitizing

Warnings

For external use only - Hands

Otc - When Using

When using this product keep out of eyes. In case of contact with eyes, flush thoroughly with water.

Avoid contact with broken skin

Do not inhale or ingest

Otc - Stop Use

Stop use and ask a doctor if skin irritation develops

Otc - Keep Out Of Reach Of Children

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

Directions

  • Wet hands thoroughly with product and rub until dry without wiping
  • For children under 6, use only under adult supervision
  • Not recommended for infants

Other Information

Do not store above 105F

May discolor some fabrics

Harmful to wood finishes and plastics

Inactive Ingredients

Water, Sorbitol, Fragrance

* Please review the disclaimer below.