Active Ingredient(S)
Benzalkonium Chloride(0.13%)
Disinfecting Wet Wipes
FDA Label NDC 81855-001
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Jiangsu Doublecotton Co.,ltd for the product Disinfecting Wet Wipes (NDC 81855-001). 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
Bacteriostat
Use
ToiletingPatients with hemorrhoids
Warnings
Ask a doctor before use if you have
Allergic hemorrhoids
Patients with allergic skin
Do Not Use
/
Otc - When Using
Ask a doctor or pharmacist before use if you are
When using this product
Toileting
Menstrual period
Travel period
Patients with hemorrhoids
Otc - Stop Use
/
Otc - Keep Out Of Reach Of Children
/
Directions
Can be thrown directly into the toilet
Can be used by the whole family
Can be used during menstrual period
Can be used by patients with hemorrhoids
Other Information
store at 0-25
Reduce sun exposure
Inactive Ingredients
Hamamelis Virginiana Top Water. EDI Purified Water. Propylene Glycol
Package Label - Principal Display Panel
81855-001-01 40CLOTH IN 1BAG
* Please review the disclaimer below.
