Active Ingredient(S)
Ethyl Alcohol 70%
The Wet Wipes
FDA Label NDC 81667-001
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Sevimli Inc. for the product The Wet Wipes (NDC 81667-001). 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(s), purpose, use, warnings, otc - when using, otc - stop use, otc - 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
Hand Sanitizer for reducing bacteria on the skin.
Warnings
For external use only.
Otc - When Using
Avoid contact with eyes. If in eyes, flush with water.
Otc - Stop Use
Stop use and ask a doctor if irritation or redness occurs.
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
Wipe hands.
Inactive Ingredients
glycerin, aloe vera, water
Disposal And Waste Handling
Discard in trash. Do not flush.
Package Label - Principal Display Panel
The Wet Wipes
Produced by Thewetwipes
1100 w cermak rd. #100
chicago/IL 60608
www.thewetwipes.com
* Please review the disclaimer below.
