Active Ingredient
BENZALKONIUM CHLORIDE 0.1%
Mediside-hand Antiseptic Tissue
FDA Label NDC 78583-702
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by You Han Greentech for the product Mediside-hand Antiseptic Tissue (NDC 78583-702). 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, direction, do not use, warnings, keep out of reach of children., stop use and ask a doctor., use, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
ANTIMICROBIAL
Direction
To dispense, peel back front label at tab
Remove towelettes as needed
Reseal pouch by pressing label firmly back into place
Do Not Use
do not flush
do not use if you are allergic to any of the ingredients
Warnings
for external sue only.
sotre away from direct sunlight or high temperature.
use caution near electric appliances to avoid electric shock.
Keep Out Of Reach Of Children.
Keep out of reach of children.
Stop Use And Ask A Doctor.
stop use and ask a doctor if irritationor or rash edvelopes and continues for more than 72 hours.
Use
peel back front label slowy.
use caution near electric appliances to avoid electric shock
Ask A Doctor
f swallowed, get medical help or contact a Poison control center right away
Other Information
7.9 in x 5.9 in (20cm x15cm )
Inactive Ingredieint
Aqua
Glycerine
Orange Sweet Ext.
Package Label
* Please review the disclaimer below.
