Active Ingredient(S)
Ethyl Alcohol 75% v/v
Alcohol Wipes
FDA Label NDC 42003-207
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Zhejiang Jiayan Daily Commodity Co., Ltd for the product Alcohol Wipes (NDC 42003-207). 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, do not use, otc - when using, otc - stop use, otc - 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
Use
Decreases bacteria on the skin
Warnings
For external use only. Flarnmable. Keep av-,ay from heat or flarne.
Do Not Use
in childr&n less than 2 months of age
on open skin wounds
Otc - When Using
When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.
Otc - Stop Use
Stop use and ask a doctor if irritation or rash occurs. These may be signs of a sefious condition.
Otc - Keep Out Of Reach Of Children
Keep out of reach o1 children. If swallowed, get medical help or contact Poison Control Center right away.
Directions
Open package. Pull wipe. Close package to retain moisture
Wet hands thoroughly with product.
Allow to dry without rinsing.
Other Information
store between 15-30C (59-86F)
Avoid freezing and exessive heat aboce 40C (104F)
Inactive Ingredients
Water
* Please review the disclaimer below.
