Gp Enmotion Antimicrobial Foam Solution
FDA Label NDC 54622-312

Full FDA labeling including Indications, Dosage, Usage, and Precautions

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Georgia-pacific Consumer Products for the product Gp Enmotion Antimicrobial Foam (NDC 54622-312). 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 other, active ingredient, purpose, use, warnings, when using this product, stop use, keep out of reach of children., and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Other

Drug Facts

Active Ingredient

Benzalkonium chloride, 0.13%

Purpose

Antiseptic

Use

Handwash to help reduce bacteria that potentially can cause disease.

Warnings

For external use only

When Using This Product

Avoid contact with eyes. In case of eye contact, flush with water.

Stop Use

if irritation or redness develops. If condition persists for more than 72 hours consult a doctor.

Keep Out Of Reach Of Children.

If swallowed, seek immediate medical attention or call a poison control center.

Directions

Wet hands, apply soap, rub hands together vigorously for at least 20 seconds.

Rinse and dry hands thoroughly.

Inactive Ingredients

Water (Aqua), Lauramine Oxide, Lauryl Betaine, Glycerin, Laurtrimonium Chloride, Sodium PCA, Tocopheryl Acetate, Aloe Barbadensis Leaf Juice, Chamomilla Recutita (Matricaria) Extract, Camellia Sinensis Leaf Extract, Avena Sativa (Oat) Kernel Extract, Euterpe Oleracea Fruit Extract, Oleth-10, Tetrasodium EDTA, Citric Acid, Green 5, Yellow 10, Fragrance

* Please review the disclaimer below.