Nitouch Alcohol Hand Sanitizer
FDA Label NDC 80437-002
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Kasa Trading, Llc for the product Nitouch Alcohol Hand Sanitizer (NDC 80437-002). 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, otc - active ingredient, otc - purpose, uses, warnings, otc - 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
Otc - Active Ingredient
Active ingredients Ethyl Alcohol 80% (v/v)
Otc - Purpose
Purpose Antiseptic
Uses
• Hand Sanitizer
• For use when soap and water are not available.
Warnings
• Flammable. Keep away from fire or flame.
• For external use only.
• When using this product: Keep out of eyes, ears and mouth. In case of contact with eyes, rinse eyes thoroughly with water. Do not inhale
or ingest.
• Do not use in children less than 2 months of age.
• Stop use and ask a doctor if irritation or a rash develops.
Otc - Keep Out Of Reach Of Children
• Keep out of reach of children. If swallowed, get medical help immediately and contact a Poison Control Center immediately.
Directions
• Apply enough product to cover hand thoroughly.
• Rub hands together, until hands feel dry. Do not rinse.
• Children under 6 years of age should be supervised when using this product.
Other Information
• Store below 105°F (40°C). May discolor some fabrics
• Avoid freezing and excessive heat above 105°F (40°C).
Inactive Ingredients
Aqua (Water), Glycerine, Fragrance, Hydrogen Peroxide, CI 42090
Packaging
Untitled (80437002 3)
* Please review the disclaimer below.
