Otc - Active Ingredient
Phenoxyethanol
Antiseptic Cleansing Wipe(0.9% Nacl) Patch
FDA Label NDC 84449-006
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Shenzhen Benliju Bio-tech Co.,ltd for the product Antiseptic Cleansing Wipe(0.9% Nacl) (NDC 84449-006). 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 otc - active ingredient, otc - purpose, indications & usage, warnings, otc - 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
Otc - Purpose
For cleansing the skin in the desired area
Indications & Usage
For cleansing the skin in the desired area
Warnings
For external use
Otc - Do Not Use
KEEP OUT OF THE REACH IOF CHILDREN.
Otc - When Using
When using this product keep out of eyes.
Otc - Stop Use
*Stop use if irritation and redness develop. If condition persists consult your health care practioner.
*Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.
Otc - Keep Out Of Reach Of Children
KEEP OUT OF THE REACH IOF CHILDREN.
Dosage & Administration
Tear open the packet, unfold the towelette. and、use it to cleanse the desired area of skin. Discardthe towelette after a single use.
Storage And Handling
Store at room temperature.
Inactive Ingredient
Sodium chloride, Deionized water
Package Label.Principal Display Panel
Package (Package)
* Please review the disclaimer below.
