Active Ingredient:
Benzalkonium Chloride 0.1%
Foaming Hand Sanitizer
FDA Label NDC 23261-100
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Sanitor Corporation for the product Foaming Hand Sanitizer (NDC 23261-100). 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, uses, warnings, when using this product, stop use and ask 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
Purpose
Antimicrobial
Uses
for hand sanitizing to decrease bacteria on the skin
recommended for repeated use
Warnings
For external use only
When Using This Product
avoid contact with eyes.
In case of contact, flush eyes with water.
Stop Use And Ask Doctor
if irritation or redness develops, or if condition persists for than 72 hours.
Keep Out Of Reach Of Children
if swallowed get medical help or contact a Poison Control Center right away.
Directions
pump enough foam to thoroughly cover your hand
rub thoroughly over all surfaces of both hands
rub hands together briskly until dry
Inactive Ingredients:
Citric Acid, Cocamidopropyl Betaine, Fragrance, Phenoxyethanol, Water
Foaming Hand Sanitizer Label
Foaming Hand Sanitizing Label (Img20201027 10242054)
* Please review the disclaimer below.
