Enmotion
FDA Label NDC 54622-686

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 Lp for the product Enmotion (NDC 54622-686). 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, uses, otc - do not use, otc - when using, otc - 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

Manufactured for
Georgia-Pacific
Professional
Atlanta, GA 30303

Active Ingredient

Ethyl Alcohol 67% v/v

Purpose

Antiseptic

Uses

  • To decrease bacteria on skin that could cause disease
  • Recommended for repeated use

Otc - Do Not Use

  • FLAMMABLE, keep away from fire or flame
  • For external use only

Otc - When Using

When using this product do not use in or near eyes.

Otc - Stop Use

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 thoroughly with product and allow to dry without wiping.

Inactive Ingredients

Water(Aqua), Aloe Barbadensis Leaf Juice, Carbomer, Diisopropylamine, Glycerin, Isopropyl Myristate, Phenoxyethanol, Tocopheryl Acetate.

Principal Display Panel - 950 Ml Bag Label

42344

enMotion®

Gel Hand Sanitizer with Moisturizers
Fragrance Free, Dye Free

2-950 mL(32.1 FL OZ)

Principal Display Panel (950 mL Bag Label)

Principal Display Panel (950 mL Bag Label)

* Please review the disclaimer below.