Eo Hand Sanitizer Spray
FDA Label NDC 54748-101

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Eo Products, Llc for the product Eo Hand Sanitizer (NDC 54748-101). 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 otc - active ingredient, otc - purpose, otc - keep out of reach of children, indications & usage, warnings:, dosage & administration, inactive ingredient, storage and handling, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Otc - Active Ingredient

Active Ingredient:

Ethanol 62%

Otc - Purpose

Purpose:

Antiseptic

Otc - Keep Out Of Reach Of Children

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

Indications & Usage

Uses: •For hand washing to decrease bacteria on skin

• Recommended for repeated use

Warnings:

  • Flammable, Keep away from fire/flame
  • For external use only
  • Do not use in eyes. If contact occurs, flush thoroughly with water.
  • Stop use and contact a doctor if redness and irritation develops and persists for more than 72 hours.

Dosage & Administration

Directions: • Wet hands thoroughly with product and allow to dry without wiping 

• Do not use other than directed.

Inactive Ingredient

Inactive Ingredients:

Purified Water, Organic Lavandula Angustifolia (Lavender) Essential Oil, Organic Echinacea Angustifolia Leaf Extract, Vegetable Glycerin, Tocopherol 

Storage And Handling

Other Information:• Store below 104°F (40°C) 

• May discolor certain fabrics.

* Please review the disclaimer below.