Active Ingredient
Ethyl Alcohol 70%
Aevi Whenever Wherever Hand Sanitizer
FDA Label NDC 62742-4203
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Allure Labs Inc for the product Aevi Whenever Wherever Hand Sanitizer (NDC 62742-4203). 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 - when using, otc - stop use, otc - keep out of reach of children, directions:, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Antimicrobial
Uses:
Helps to reduce bacteria on the skin. For repeat use.
Warnings
For external use only. Flammable, keep away from heat and flame. Do not store above 104°F/40°C.
Otc - When Using
When using this product
• Keep out of eyes. In case of contact with eyes, flush thoroughly with water.
• Avoid contact with broken skin.
Otc - Stop Use
Stop use and ask a doctor if skin irritation develops.
Otc - Keep Out Of Reach Of Children
Keep out of reach of children. If product is swallowed, get medical help or contact a Poison Control Center immediately.
Directions:
Apply all over your hands and allow to dry. Do not rinse off. For children under 6, use only under adult supervision. Not recommended for infants.
Inactive Ingredients
Aqua (Water), Glycerin, Aloe Barbadensis (Aloe Vera) Leaf Juice*, Pinus Sylvestris Leaf (Nordic Pine) Oil, Eucalyptus Globulus Leaf Oil*, Rosmarinus Officinalis (Rosemary) Oil, Linalool, Limonene.
Package Label.Principal Display Panel
Aevi Wellness, Inc
251 Little Falls Drive
Wilmington, DE 19808
Made in USA
Imgavhs2oz (Imgavhs2oz)
* Please review the disclaimer below.
