Active Ingredient
Alcohol 80% v/v.
Skintillate Hand Sanitizer
FDA Label NDC 75306-005
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 75306-005). 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, use, warning, ask doctor, keep out of reach of children., directions, inactive ingredients, 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
Warning
For external use only
When using this product avoid contact with eyes.
Flammable. Keep away from heat and flame.
Ask Doctor
Stop use and consult a healthcare professional if irritation develops.
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.
Inactive Ingredients
Water, Isopropyl alcohol, Glycerin, Hyaluronic Acid, Bergamot leaf oil, Lavender Flower, Hydrogen Peroxide, Centella Asiatica Extract, Sodium pyruvate
Other Information
Store at 68 to 70 F (20 to 25 C). May discolor certain fabrics on surfaces
Questions?
1-844-800-6858
Package
Image Description (Image)
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