Elyptol Antimicrobial Hand Gel
FDA Label NDC 69343-121

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Elyptol Inc. for the product Elyptol Antimicrobial Hand Gel (NDC 69343-121). 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, 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

Drug Facts

Active Ingredient

Ethyl Alcohol 70% v/v

Purpose

Antiseptic

Uses

  • To decrease bacteria on skin.
  • Recommended for repeated use.

Warnings

For external use only.

Flammable. Keep away from sources of fire or flame.

When using this product

keep away from eyes. In case of eye contact, rinse eyes with water.

Stop use and ask a doctor if

redness or irritation develops. If issues persist, seek medical attention.

Keep Out Of Reach Of Children.

If swallowed, seek medical advice or contact a Poison Control Center immediately.

Directions

  • Apply Elyptol liberally onto palm of hand.
  • Cover hands with product by thoroughly rubbing and allow to air dry without wiping.
  • Use undiluted.
  • Supervise children under 6 years.
  • Not recommended for infants.

Other Information

• Store below 86°F/30°C.
• Keep out of direct sunlight.

Inactive Ingredients

Aqua (Purified Water), Eucalyptol, Glycerin, Hydroxypropylcellulose, Piroctone Olamine

Questions?

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Packaging

Image Description (69343121 1)

Image Description (69343121 1)

Image Description (69343121 2)

Image Description (69343121 2)

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