Active Ingredient
Ethyl Alcohol 75% ± 5 % v/v.
Lovali Hand Sanitizer
FDA Label NDC 75007-003
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Yirong Trading (nanjing) Co., Ltd for the product Lovali Hand Sanitizer (NDC 75007-003). 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 ingredient, 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
Antimicrobial
Use
Reduces bacteria and viruses on the hands that may cause disease.
Warnings
Flammable. Keep away from open flame.
When using this Product: Avoid contact with eyes and broken skin. In case of eye contact, flush with plenty of water and seek medical advice.
Stop use and ask a doctor if irritation or redness develops.
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
Wet hands thoroughly with product and rub into skin until dry.
Children 6 years and younger need adult supervision when using this product.
Inactive Ingredients
Water (Aqua). Glycerin, Propylene Glycol, Carbomer, Fragrance, Aminomethyl Propanol,Aloe Barbadensis (Aloe Vera) Gel,Tocopheryl Acetate (Vitamin E)
Package Label - Principal Display Panel
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