Xpro Antiseptic Hand Sanitizer Gel
FDA Label NDC 77939-000
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Savone Sa for the product Xpro Antiseptic Hand Sanitizer (NDC 77939-000). 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, do not use, stop use and ask a docotor if, keep out of reach of children, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Active Ingredient
Ethyl alcohol 70%
Purpose
Antiseptic
Use
for hand washing to decrease bacteria on the skin
Warnings
For external use only
Flammable, keep away from fire and flame
Do Not Use
in the eyes
Stop Use And Ask A Docotor If
- irritation and redness develop
- condition persists for more than 72 hours
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
Other Information
keep in a dry place at room temperature
Inactive Ingredients
aloe vera leaf extract, carbomer, isopropyl myristate, propylene glycol, triethanolamine, water
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