Hand Sanitizer
FDA Label NDC 77066-777

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Enlightened Llc for the product Hand Sanitizer (NDC 77066-777). 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, directions, inactive ingredients, package label.principal display panel, 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% W/W

Purpose

ANTISEPTIC

Uses

TO DECREASE BACTERIA ON THE SKIN. RECOMMENDED FOR REPEATED USE.

Warnings

Flammable, keep away from fire or flames

For external use only

When using this product

  • Do not use near the eyes.
  • In case of contact, flush thoroughly with water

    • Stop use and ask doctor if

    • Irritation or redness develop and persist for more than 72 hours

Otc - Keep Out Of Reach Of Children

Keep out of reach of children. If swallowed, get medical help or contact Poison Control Center immediately

Directions

Spray product on both sides of your hands and rub hands together briskly until dry. Spray on surfaces to be sanitized. Children under the age of six should be supervised when using this product. For human use only.

Inactive Ingredients

Water, Aloe Leaf Juice, Witch Hazel, Lavender – Lavandula Angsutifolia (Lavender) Essential Oil, Eucalyptus – Eucalyptus Globulus Essential Oil

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