Active Ingredient
Ethyl Alcohol 70%
Ethyl Alcohol
FDA Label NDC 67151-738
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 Products, Llc for the product Ethyl Alcohol (NDC 67151-738). 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, flammable, do not use, stop use and ask a doctor, 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
Purpose
Antiseptic
Uses
- Hand sanitizing wipes to help reduce bacteria on the skin.
Warnings
For External use only.
Flammable
Keep away from fire or flame.
Do Not Use
- in or near the eyes
- on open skin wounds or burns
Stop Use And Ask A Doctor
- if irritation or redness develops
- condition persists or get worse
Keep Out Of Reach Of Children
If swallowed, get medical help or contact a Poison Control Center immediately.
Directions
- Pull back canster lid
- Remove wipe
- Close canister lid
- Keep lid closed to retain moisture
- Wet hands thoroughly with product and allow to dry without wiping
- For single use only. Discard individual wipe after use
Other Information
- Store at room temperature
- Dispose of used wipe in trash, do not flush into toilet.
Inactive Ingredients
Water, Propylene Glycol, Glycerin, Fragrance, Benzalkonium chloride, Tocopherol Acetate, Citric Acid, Aloe Barbadensis Leaf Juice
Principal Display Panel
WAXIE
Hand Sanitizing Wipes
70% Alcohol Based
Kills 99.9% of germs
Box (67151 737 02)
12/240 CT CANISTERS
* Please review the disclaimer below.
