Ea Instant Hand Sanitizer
FDA Label NDC 78233-013

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by National Travel Product, Inc for the product Ea Instant Hand Sanitizer (NDC 78233-013). 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 ingredient, purpose, uses, warnings, when using this product:, stop use and ask a doctor if:, keep out of reach of children., and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Drug Facts

Active Ingredient

Ethyl Alcohol 75%

Purpose

Antiseptic

Uses

  • For hand sanitizing to decrease bacteria on the skin
  • Recommended for repeated use

Warnings

For external use only

When Using This Product:

avoid contact with eyes. In case of eye contact, flush eyes with water.

Stop Use And Ask A Doctor If:

irritation or redness develops, or if condition persists for more than 72 hours.

Keep Out Of Reach Of Children.

If swallowed get medical help or contact a Poison Control Center right away.

Directions

  • Pump appropriate amount of sanitizer on to hands and rub together until dry. Use as needed. For children under 6, use with adult supervison. Not recommended for infants.

Inactive Ingredients:

Water, Aloe Barbadensis Leaf Extract, Acrylates/C10-30 alkyl Acrylate Crosspolymer, Tetrahydroxypropyl Ethylenediamine.

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