Active Ingredient
Ethyl Alcohol 75%
H2one Gel
FDA Label NDC 75742-006
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 H2one (NDC 75742-006). 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, stop use and ask a doctor, 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
Antiseptic
Uses
To help reduce bacteria on the skin
Warnings
For external use only
Avoid contact with eyes. If contact occurs, rinse thoroughly with water.
FLAMMABLE, KEEP AWAY FROM FIRE
Stop Use And Ask A Doctor
Stop use and ask a doctor if rash or irritation or redness develops and lasts.
Keep Out Of Reach Of Children
If product is swallowed, get medical help or contact a Poison Control Center right away.
Directions
Place 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.
Other Information
Store below 110F(43C)
May discolor certain fabrics or surfaces
Inactive Ingredients
Aqua
Glycerin
Carbomer
Aloe Vera
Triethanolamine
Vitamin E
Label
Label (Label)
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