Active Ingredient
Ethyl Alcohol 80%
Lilkoi Hand Sanitizer
FDA Label NDC 75306-007
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by D-time Limited Liability Company for the product Lilkoi Hand Sanitizer (NDC 75306-007). 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, lilkoi hand sanitizer, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Antiseptic skin cleanser
Uses
For personal hand hygiene to help prevent the spread of bacteria.
Warnings
For external use only.
Flammable. Keep away from open flame and sources of heat.
When using this product avoid contact with eyes. If contact occurs, rinse thoroughly with water.
Stop use and consult a healthcare professional if irritation develops.
Otc - Keep Out Of Reach Of Children
Keep out of reach of children.If swallowed, contact a Poison Control Center or get medical help right away.
Directions
Adults and children over 2 years: For occasional and personal domestic use Supervise children when they use this product ∙ Spray onto hands and rub thoroughly for at least 30 seconds. Allow to dry.
Other information
Store at 68° to 70° F (20° to 25° C).
May discolor certain fabrics or surfaces.
Questions? 1-844-800-6858
Inactive Ingredients
Water, Glycerin, Sweet almond oil, Lavender Flower Oil, Hydrogen Peroxide, Sodium pyruvate.
Lilkoi Hand Sanitizer
Image Description (Lilkoi22)
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