Active Ingredients
Ethyl alcohol 70% by volume
Ethyl Alcohol
FDA Label NDC 67151-717
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Progressive for the product Ethyl Alcohol (NDC 67151-717). 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 ingredients, purpose, uses, warnings, do not use, stop use and ask a doctor, 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
- For hand sanitizing to decrease bacteria on the skin.
- Apply topically to the skin to help prevent cross contamination.
- Not recommended for repeated use.
- Dries in seconds.
Warnings
- For external use only.
Do Not Use
- in or near the eyes
- on open skin wounds or burns
Stop Use And Ask A Doctor
- if irritation and redness develop
- condition persists for more than 72 hours.
Directions
- Pull back reseal label.
- Remove wipe.
- Reseal label.
- Keep label closed to retain moisture.
Other Information
- Store at room temperature.
- Dispose of used wipe in trash, do not flush into toilet.
Inactive Ingredients
Aloe barbadensis leaf juic, Glycerin, Isopropanol, Propanediol, Tocopheryl acetate, Water.
Keep Out Of Reach Of Children.
If swallowed, get medical help or contact a Poison Control Center right away.
Principal Display Panel
wipesplu
HAND SANITIZING WIPES
- Kills 99.9% of germs
80CT
PRE-MOISTENED TOWELETTES
* Please review the disclaimer below.
