Active Ingredient
Alcohol (60%)
Centecassol S.o.s Sanitizer
FDA Label NDC 73800-101
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Hansolbio Co., Ltd for the product Centecassol S.o.s Sanitizer (NDC 73800-101). 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, directions, keep out of reach of children, inactive ingredients, centecassol s.o.s sanitizer (200ml), and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Antibacterial
Uses
Uses Hand sanitizer for decreasing bacteria on skin
Warnings
For external use only
Do not use if you are allergic to any of the ingredients
When using this product avoid contact with eyes. If contact occurs, rinse eyes thoroughly with water. avoid contact with broken, irritated, or itching skin. Do not puncture or incinerate.
Stop use and ask a doctor ifirritation or redness develops and condition persists for more than 72 hours
If pregnant or breast-feeding, ask a health professional before use.
Directions
Take appropriate amount onto your hand and spread it all the way to fingertips. Rub the contents until it dries
Keep Out Of Reach Of Children
If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) right away.
Inactive Ingredients
Water, Centella Asiatica Extract, Carbomer, Triethanolamine, Melaleuca Alternifolia (Tea Tree) Leaf Oil
* Please review the disclaimer below.
