Otc - Active Ingredient
Ethyl Alcohol (Alcohol) 62% (w/w)
Fresh Water Hand Sanitizer
FDA Label NDC 74773-0013
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Theskinfactory Co., Ltd. for the product Fresh Water Hand Sanitizer (NDC 74773-0013). 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 otc - active ingredient, inactive ingredient, otc - purpose, otc - keep out of reach of children, indications & usage, warnings, dosage & administration, 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
Inactive Ingredient
Glycerin, Carbomer, Green Tea Extract, Aloe Extract, L-Menthol, Aminomethyl Propanol, Water
Otc - Purpose
Antimicrobial
Hand gel for cleaning and moisturizing the hand
Otc - Keep Out Of Reach Of Children
KEEP OUT OF REACH OF THE CHILDREN
Indications & Usage
Store under 30°C (86°F)
Warnings
For external use only.
Flammable, keep away from fire or flame.
When using this product keep out of eyes. If contact with eyes occurs, rinse promptly and thoroughly with water.
Stop use and ask a doctor if significant irritation or sensitization develops.
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
Dosage & Administration
- Put enough product in your palm to thoroughly cover your hands
- Rub hands together briskly until dry
- Children under 6 years of age should be supervised when using this product
* Please review the disclaimer below.
