Evergreen
FDA Label NDC 79881-020
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Ela Kozmetik Ve Hijyenik Urunleri Sanayi Ticaret Limited Sirketi for the product Evergreen (NDC 79881-020). 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
Benzalkonium chloride 0.13%
Purpose
Antibacterial
Uses
• hand sanitizer to decrease bacteria on the skin
• recommended for repeated use
• for use when soap and water are not available
Warnings
For external use only
Do not use
• on children less than 2 years of age
• on open skin wounds
When using this product do not get into eyes. In case of contact, rinse eyes thoroughly with water
Stop use and ask a doctor if
• irritation and redness develop
• condition persists for more than 72 hours
Keep Out Of Reach Of Children.
If swallowed, get medical help or contact a Poison Control Center right away
Directions
• wet hands thoroughly with product and allow to dry without wiping
• supervise children under 6 years of age when using this product to avoid swallowing
Other Information
• store between 15-30°C (59-86°F)
• avoid freezing and excessive heat above 40°C (104°F)
Inactive Ingredients
water, phenoxyethanol, benzoic acid, dehydroacetic acid, cetearyl isononanoate, ceteareth-20, cetearyl alcohol, glyceryl stearate, ceteareth-12, cetyl palmitate, cocamidopropyl betaine, fragrance, glycerin, tetrasodium EDTA, allantoin, panthenol, disodium laureth sulfosuccinate
Packaging
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