Active Ingredient
Active ingredient purpose
Benzalkonium Chloride 0.1% Antimicrobial
New Wave Sanitizer Wipe
FDA Label NDC 54860-328
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 Lantern Science Co.,ltd. for the product New Wave Sanitizer Wipe (NDC 54860-328). 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 drug facts, active ingredient, use, warnings, when using this product, stop use and ask a doctor, 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
Use
for hand sanitizing to decrease bacteria on skin
recommended for repeated use.
Warnings
For external use only.
When Using This Product
Avoid contact with eyes.In case of eye contact,flush eyes with water.
Stop Use And Ask A Doctor
if irritation or redness develops,or if condition 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
remove and unfold wipe
wipe hands thoroughly and allow to dry
do not flush
Inactive Ingredient
Aqua,phenoxyethanol,polysorbate 20,disodium EDTA,sodium citrate,fragrance.
Usage
Remove and unfold wipe
wipe hands thoroughly and allow to dry.
do not flush
* Please review the disclaimer below.
