Active Ingredient
Benzalkonium Chloride, 0.13%
Benzalkonium Chloride Towelette
FDA Label NDC 72766-003
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Yangzhou Suxiang Medical Instrument Co., Ltd. for the product Benzalkonium Chloride Towelette (NDC 72766-003). 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, do not use, stop use and ask a doctor if, 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
First Aid Antiseptic
Uses
First Aid Antiseptic
Warnings
For External Use Only
Do Not Use
For deep puncture wounds, animal bites or serious burns
In the eyes
Over large areas of the body
Stop Use And Ask A Doctor If
if irritation and redness develops and persists for more than 72 hours
Keep Out Of Reach Of Children
If swallowed, get medical help or contact a Poison Control Center right away.
Directions
Open packet and use as a washcloth.
As a first aid antiseptic
Clean affected area
Apply 1 to 3 times daily
May be covered with a sterile bandage
If bandaged, let dry first
Other Information
Store at room temperature
Avoid excessive heat
Inactive Ingredients
Purified Water
Greight Benzalkonium Chloride Towelette - 1Pc
Gr8-bct-001 (Gr8 Bct 001)
* Please review the disclaimer below.
