Pureus
FDA Label NDC 78286-725
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Winmedia24 for the product Pureus (NDC 78286-725). 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 drug facts, active ingredient, purpose, use, warnings, otc - keep out of reach of children, directions, inactive ingredients, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Active Ingredient
Ethyl Alcohol 62%
Purpose
Antimicrobial
Use
for hand-washing to decrease on the skin, only when water is not available
Warnings
Flammable, Keep away from fire and flames
For External use only
When using this product
▪do not get into eyes
▪if contact occurs, rinse eyes thoroughly with water
Stop use and ask a doctor if
▪irritation and redness develop
Otc - Keep Out Of Reach Of Children
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away
Directions
▪ wet hands thoroughly with product and allow to dry without wiping
Inactive Ingredients
Distilled water, Glicerine, Vitamin E
Other
• Kills 99.9% of Germs
• Antimicrobial Formula
• Moisturizing
DYE FREE • PHOSPHATE FREE • PARABEN FREE
Made in USA
Distributed by:
Winmedia24, Inc.
Studio City, CA91604
213-713 0095
www.winmedia24.com
Packaging
Image (Wmd)
* Please review the disclaimer below.
