Other
Drug Facts
Alcohol Wipes Cloth
FDA Label NDC 81079-002
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Shaoxing Elite Bio-tech Co.,ltd. for the product Alcohol Wipes (NDC 81079-002). 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 other, active ingredient(s), purpose, use, warnings, do not use, otc - when using, otc - stop use, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Active Ingredient(S)
Alcohol 75% v/v
Purpose
Antiseptic
Use
For hand sanitizing to decrease bacteria on skin.
Warnings
For external use only. Flammable: Keep away from fire or flame.
Do Not Use
In children less than 2 months of age.
On open skin wounds.
Otc - When Using
When using this product avoid contact with eyes and mouth. If in eyes，flush thoroughly with water.
Otc - Stop Use
Discontinue use and contact a doctor if irritation and redness develop and conditions persist for more than 72 hours.
Otc - Keep Out Of Reach Of Children
Keep out of reach of children unless under adult supervision. If swallowed, get medical help or contact a Poison Control Center right away.
Directions
Open the lid, tear open packet, remove wipe.
Wet hands thoroughly with product and let hands air dry.
Throw used wipe in trash.
Do not flush.
Other Information
Store between 15-30 °C (59-86 °F).
Avoid freezing and excessive heat above 40 °C (104 °F).
Inactive Ingredients
Water.
Package Label - Principal Display Panel
NDC:81079-002-01
10 (10)
20 (20)
40 (40)
60 (60)
80 (80)
100 (100)
* Please review the disclaimer below.
