Active Ingredient
Ethyl Alcohol 75% v/v.
Green Island Gel
FDA Label NDC 75742-002
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Zhejiang Guoyao Jingyue Aerosol Co., Ltd. for the product Green Island (NDC 75742-002). 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 active ingredient, purpose, uses, warnings, do not use, 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
Purpose
Antimicrobial
Uses
- for the surface of hands or other objects disinfection
- recommended for repeated use
Warnings
For external use only.
Flammable, keep away from heat or flame
Avoid contact with eyes or mouth.
If irritation or redness & swelling occurs, discontinue use immediately.
Do Not Use
if you are allergic to alcohol
Otc - Keep Out Of Reach Of Children
Keep out of reach of children.
Directions
- Apply on the surface of hands or other objects to be disinfected, stay 3 minutes until dry naturally.
Other Information
- Store at 20°C to 25°C (68° to 77°F)
- may discolor certain fabrics
Inactive Ingredients
water
* Please review the disclaimer below.
