Foaming Hand
FDA Label NDC 82110-001
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Shiby Inc for the product Foaming Hand (NDC 82110-001). 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 drug facts, active ingredient, purpose, use, warning, when using this product, 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
Active Ingredient
0.13% Benalkonium chloride
Purpose
Antibacterial
Use
helps eliminate bacteria on hands
Warning
For external use only
When Using This Product
do not use in near the eyes. In case of contact, rinse eyes thoroughly with water.
Keep Out Of Reach Of Children,
except under adult supervision. If swallowed, get medical help or contact a Poison Control Center right away.
Directions
Wash hands and rinse
Inactive Ingredients
Water (Aqua), Sodium Laureth Sulfate, Cocamidopropyl Betaine, Glycerin, Coconut Oil Diethanolamide, Sodium Lauryl Sulfate, Phenoxyethanol, Parfume, Sodium Benzoate, Citric Acid
Package Labeling:
Bottle (Bottle)
* Please review the disclaimer below.
