Active Ingredient
Benzalkonium Chloride 0.1%
Protect U Guard Antibacterial Foaming
FDA Label NDC 71788-001
9 label sections · Submitted to the FDA by Protect U Guard, Llc · Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Protect U Guard, Llc for the product Protect U Guard Antibacterial Foaming (NDC 71788-001). 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 active ingredient, purpose, use, warnings, otc - when using, otc - stop use, otc - 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
Skin Antimicrobial
Use
Reduces amount of bacteria on hands
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 of 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.
Otc - When Using
When using this product avoid contact with eyes. In case of eye contact, flush eyes with water.
Otc - Stop Use
Stop use and ask a doctor if irritation or redness develops, or if condition persists for more than 72 hours.
Otc - Keep Out Of Reach Of Children
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
Directions
Apply a palmful to hands and forearms.
Scrub thoroughly for at least fifteen seconds
Rinse completely and dry.
Inactive Ingredients
Water, Lauramine Oxide, Glycerin, PEG-120 Methyl Glucose Dioleate, Fragrance
* Please review the disclaimer below.
