Active Ingredient(S)
Benzalkonium Chloride 0.1%,DDAC 0.1%
Sterilized Wet Wipes
FDA Label NDC 78447-001
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Zhejiang Baojia Biotechnology Co., Ltd. for the product Sterilized Wet Wipes (NDC 78447-001). 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(s), warnings, do not use, when using this product, stop use and ask a doctor, keep out of the 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(S)
Health care personnel hand rub to help reduce bacteria that potentially can cause diseaze.
Warnings
For extemal use only, Avoid extreme temperature
Do Not Use
In children less than 6 months of age
On open skin wounds
When Using This Product
Keep out of eyes and mouth, in case of contact with eyes,rinse eyes thoroughly with water.
Stop Use And Ask A Doctor
lf iirritation or rash occurs, these may be signs of a serious condition.
Keep Out Of The Reach Of Children
if swallowed,get a medical help or call a poison control center right away.
Directions
pull out the wipes to rub all surfaces of hands,.
Supervise children under 6 years of age when using this product to avoid swallowing.
Other Information
Store between 5-30℃(41-86F)
Avoid freezing and excessive heat above 40(104F)
Inactive Ingredients
Glycerin, Phenoxyethanol Ethylhexylglycerin, Propylene Glycol,Purfied Water.
* Please review the disclaimer below.
