Active Ingredient(S)
Benzalkonium Chloride 0.2%
Antibacterial Wipes
FDA Label NDC 40562-015
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Anhui Hanbon Daily Chemical Co., Ltd. for the product Antibacterial Wipes (NDC 40562-015). 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
Antimicrobial
Use
For hand sanitizing to decrease bacteria.
Warnings
For external use only.
Keep out of eyes. In case of eye contact, rinse eyes with water.
Keep out of sunlight.
Otc - When Using
If eye contact occurs, rinse thoroughly with water.
Otc - Stop Use
Stop use and ask a doctor if rednes or irritation develops;
Otc - Keep Out Of Reach Of Children
If swallowed get medical help or contact a Poison Control center right away.
Directions
Peel back flap on front to pull out a towelette. Reseal the flap. No need to rinse.
Inactive Ingredients
Water, Glycerin, Propylene Glycol, Polyaminopropyl Biguanide, Phenoxyethanol, Iodopropynyl Butylcarbamate, Green Tea Extract.
Package Label - Principal Display Panel
100 PATCH in 1 PACKET NDC: 40562-015-01
100pcs Label (100pcs)
* Please review the disclaimer below.
