enMotion Foam

Manufacturer
Georgia-Pacific Consumer Products LP | Nice-Pak Products, LLC
Effective date
2026-02-04
Label type
HUMAN OTC DRUG LABEL
Version
14
Source
full-release
Hydrated at
2026-06-01 01:37:04

Label at a glance#

ProductenMotion Foam High Frequency Use
Active ingredientALCOHOL
Label structure12 sections

Indications and uses

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

Dosage and administration

Wet hands thoroughly with product and allow to dry without wiping.

Label contents#

Full prescribing information#

Claims

SPL UNCLASSIFIED SECTION

enMotion

High Frequency Use

Foam Hand Sanitizer

Fragrance Free • SKU 42336

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 70% v/v

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

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

Warnings

WARNINGS SECTION

FLAMMABLE, keep away from fire or flame

For external use only

When using this product

OTC - WHEN USING SECTION

do not use in or near eyes.

Stop use and ask a doctor

OTC - STOP USE SECTION

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

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

  • Wet hands thoroughly with product and allow to dry without wiping.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Isopropyl Alcohol, PEG-12 Dimethicone, Glycerin, Hydrolyzed Jojoba Esters,Caprylic/Capric Triglyceride, Panthenol, Isopropyl Myristate, Aloe Barbadensis Leaf Juice, Chamomilla Recutita (Matricaria) Flower Extract, Camellia Sinensis Leaf Extract, Avena Sativa (Oat) Kernel Extract, Euterpe Oleracea Fruit Extract, Butylene Glycol, Bisabolol, Phenoxyethanol, Citric Acid, Sodium Benzoate, Potassium Sorbate, Acetyl Hexapeptide-49

ADVERSE REACTION

ADVERSE REACTIONS SECTION

Manufactured for Georgia-Pacific Consumer Products LP. Atlanta, GA 30303

Questions? Call 1-866-HELLOGP (435-5647)

or visit us online at www.gppro.com

(c) 2021 GP PRO. All rights reserved.

alcohol permit SDS-MO-20068, DSP-MO-28, DSP-MO-20087

principal display panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

High Frequency Use

Foam Hand Sanitizer

G-1000522-PRDRevA16

1000 mL (33.8 FL OZ)

image descriptionimage descriptionimage descriptionimage description

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
616805ethanol 70 % Topical FoamPSN14
616805ethanol 0.7 ML/ML Topical FoamSCD14
616805ethanol 70 % Topical FoamSY14

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
54622-486-01enMotion FoamHigh Frequency Use1000 mL in 1 BOTTLE, DISPENSINGSOLUTION100014

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 23 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
54622-48654622-486-01

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 21 matching rows.

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
enMotion Foam High Frequency UseETHYL ALCOHOLGeorgia-Pacific Consumer Products LPe56f5a94-0be1-487b-ad95-c1fe74c824ee2026-02-04Warnings, Adverse reactionsExact identifier
ndc (package): 54622-486-01
ndc (product): 54622-486
ndc11 (package): 54622048601
spl id: 4a0372c0-7f0f-3e75-e063-6394a90aa9f1
spl set id: e56f5a94-0be1-487b-ad95-c1fe74c824ee

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.