Otc - Active Ingredient
benzalkonium
Ezpharm Hand Sanitizing Tissue
FDA Label NDC 58474-001
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Wooil C&tech.corp for the product Ezpharm Hand Sanitizing Tissue (NDC 58474-001). 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 otc - active ingredient, inactive ingredient, otc - purpose, otc - keep out of reach of children, indications & usage, warnings, dosage & administration, package label.principal display panel, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Inactive Ingredient
Water, Glycerin, Polysorbate 80, Sodium Benzonate, Citric Acid, Maltodextrin, Aloe Barbadensis Leaf Juice Powder, Fragrance, Tocopheryl Acetate
Otc - Purpose
■ To decrease bacteria on the skin that could cause disease
■ Recommended for repeated use
Otc - Keep Out Of Reach Of Children
KEEP OUT OF REACH OF THE CHILDREN
Indications & Usage
■ Wipe hands thoroughly with product and allow to dry.
■ Discard wipe in trash. Do not flush.
Warnings
■ keep out of eyes. In case of contact with eyes, flush thoroughly with water.
■ avoid contact with broken skin.
■ do not inhale or ingest.
Dosage & Administration
external use only
Package Label.Principal Display Panel
Label (Label)
* Please review the disclaimer below.
