Active Ingredients
Alcohol (80%)
Ethyl Alcohol (75%), Isopropyl Alcohol (5%)
Skintillate Hand Sanitizer
FDA Label NDC 75306-003
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 Skintillate Hand Sanitizer (NDC 75306-003). 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 ingredients, purpose, use, 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
Purpose
Antiseptic skin cleanser
Use
For personal hand hygiene to help prevent the spread of bacteria.
Warnings
For external use only.
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.
Flammable. Keep away from heat and flame.
Otc - Keep Out Of Reach Of Children
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center 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.
Inactive Ingredients
Water, Hydrogen Peroxide , Glycerin, Hyaluronic Acid, Bergamot leaf oil, Lavender Flower Oil, Centella Asiatica Extract, Sodium pyruvate
Other information
Store at 680 to 700 F (200 to 250C). May discolor certain fabrics or surfaces.
Questions? 1-844-800-6858
Package Label - Principal Display Panel
Label 1 (Label)
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