Active Ingredients
Ethyl Alcohol 70.0%
Raon Hand Sanitizer Gel
FDA Label NDC 79487-202
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Liz Corporation Co., Ltd for the product Raon Hand Sanitizer Gel (NDC 79487-202). 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 ingredients, purpose, use, warnings, when using this product, stop use and ask a doctor if, 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
ANTISEPTIC
Use
Hand sanitizer to decrease bacteria on the skin that could cause disease
Warnings
For external use only. Flammable. Keep away from heat and flame.
When Using This Product
Keep out of eyes. In case of contact with eyes, flush thoroughly with water. Avoid contact with broken skin. Do not inhale or ingest.
Stop Use And Ask A Doctor If
skin irritation or rash develops.
Keep Out Of Reach Of Children
If swallowed, get medical help or contact a Poison Control Center right away.
Directions
Place enough product on hands to cover all surfaces. Rub hands together until dry
Superevise children under 6 years of age when using this product to avoid swalloing.
Other Information
Store between 15-30°C (59-86°F)
Avoid Freezing and excessive heat above 40°C (104°F)
Inactive Ingredients
Water, Butylene Glycol, Carbomer, Triethanplamine, Aloe Barbadensis Leaf Extract, Artemisia Vulgaris Extract
Package Label
* Please review the disclaimer below.
