Active Ingredient
Ethyl Alcohol 75.0%v/v
Hand Sanitizer
FDA Label NDC 78403-001
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Guangzhou Cangty Biotechnology Co., Ltd. for the product Hand Sanitizer (NDC 78403-001). 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, do not use, stop use and ask a doctor if, keep out of reach for children, directions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Antimicrobial
Uses
for handwashing to decrease bacteria on the skin.
recommended for repeated use.
Warnings
For external use only.Flammable. Keep away from heat and flame.
Do Not Use
in the eyes.In case of contact,rinse eyes thoroughly with water.
Stop Use And Ask A Doctor If
irritation and redness develop and persistfor more than 72 hours.
Keep Out Of Reach For Children
If swallowed,get medical help or contact a Poison Control Center right away.
Directions
wet hands thoroughly with product briskly rub hands together until dry. Supervise children under 6 years in the use of this product.
Other Information
store at 20℃ to 25℃(68° to 77°F）
may discolor certain fabrics.
Inactive Ingredients
Water,Glycerin, Carbomer,Aloe Vera,Triethanolamine,Vitamin E.
* Please review the disclaimer below.
