Elyptol Antimicrobial Moisturizing Hand Sanitizer
FDA Label NDC 69343-222
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 Moisturizing Hand Sanitizer (NDC 69343-222). 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
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 out of eyes
• In case of eye contact, rinse eyes with water.
Stop use and ask a doctor if redness or irritation develops and persist for more than 72 hours
Keep Out Of Reach Of Children
If swallowed, get medical help or contact a Poison Control Center immediately
Directions
• Apply Elyptol liberally onto palm of hand, thoroughly rubbing & 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, Vegetable Glycerin, Piroctone Olamine
Packaging
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