Everyone Hand Sanitizer Spray
FDA Label NDC 54748-601
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 Everyone Hand Sanitizer (NDC 54748-601). 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 drug facts, active ingredients:, purpose:, uses:, warnings:, • keep out of reach of children., directions:, other information:, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Active Ingredients:
Ethanol 62%
Purpose:
Antiseptic
Uses:
• For hand washing to decrease bacteria on skin
• Recommended for repeated use
Warnings:
• Flammable, keep away from fire or flame.
• For external use only
• Do not use in eyes. If contact occurs, flush thoroughly with water.
• Stop use and ask a doctor if redness and irritation develops and persists for more than 72 hours.
• Keep Out Of Reach Of Children.
If swallowed, get medical help or contact the Poison Control center right away.
Directions:
• Wet hands thoroughly with product and allow to dry without wiping.
• Do not use other than directed.
Other Information:
• Store at room temperature 20°-25°C (68°F - 77°F)
• May discolor certain fabrics.
Inactive Ingredients:
Water, Citrus Medica Limonum (Lemon) Peel Oil, †Gamma Octalactone, †Gamma Nonalactone, †Heliotropine, †Vanillin, **Aloe Barbadensis Leaf Juice, **Matricaria Recutita (Chamomile) Flower Extract, **Calendula Officinalis Flower Extract, **Camellia Sinensis (White Tea) Leaf Extract, Glycerin, *Limonene
*component of essential oil **organic †component of organic coconut flavor extract
Packaging
Image (54748601)
* Please review the disclaimer below.
