Handy Pocket Sanitizer Mist
FDA Label NDC 81601-003

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Cellicon Lab Inc. for the product Handy Pocket Sanitizer Mist (NDC 81601-003). 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, other information, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Active Ingredient

Ethyl alcohol 70.3% w/w

Purpose

Antimicrobial

Use

  • Hand sanitizer to help decrease bacteria on the skin

Warnings

Flammable. Keep away from fire 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.

Other Information

  • Store below 110°F (43°C)
  • May discolor certain fabrics or surfaces

Directions

Wet hands thoroughly with product and allow to dry without wiping

Inactive Ingredients

Water, Glycerin, Octyldodeceth-16, Fragrance, Butylene Glycol, Limonene, Salicylic Acid, Sodium Citrate, Linalool, Hexyl Cinnamal, Centella Asiatica Extract, 1,2-Hexanediol, Scutellaria Baicalensis Root Extract, Polygonum Cuspidatum Root Extract, Portulaca Oleracea Extract, Camellia Sinensis Leaf Extract, Glycyrrhiza Glabra (Licorice) Root Extract, Chamomilla Recutita (Matricaria) Flower Extract, Rosmarinus Officinalis (Rosemary) Leaf Extract, Oligopeptide-145

* Please review the disclaimer below.