Active Ingredient
Ethyl Alcohol 75%v/v
Pyurx
FDA Label NDC 75186-008
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Huizhou Duomei Daily Necessities Co.,ltd for the product Pyurx (NDC 75186-008). 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, use, warnings, do not use, 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
- For hand sanitizing 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
Do not use in the eyes. In case of contact, rinse eyes thoroughly with water.
Do not use on children less than 2 months of age.
Stop Use And Ask A Doctor If
Stop use and ask a doctor if
- Irritation or redness develop and persist for more than 72 hours.
- Swallowed, get medical help or contact a posion control center right away.
Keep Out Of Reach Of Children
Children must be supervised when using of this product.
Directions
- Place enough product in your palm to cover hands and rub hands together 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(Water), Glycerin, Carbomer, Triethanolamine,Aloe,Tocopheryl Acetate(Vitamin E)
Label
Label (Label)
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