enMotion Foam Sanitizer with Moisturizers Fragrance Free

Manufacturer
Georgia Pacific Consumer Products | Accupac, LLC
Effective date
2021-03-23
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:40:37

Label at a glance#

ProductenMotion Foam Sanitizer with Moisturizers Fragrance Free
Active ingredientALCOHOL
Label structure11 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#

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

OTC - WHEN USING SECTION

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

OTC - STOP USE SECTION

Stop use and ask a doctor 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, Blue 1, Yellow 5.

*may contain this ingredient

Rear Label Text

SPL UNCLASSIFIED SECTION

enMotion®

Foam Hand Sanitizer with Moisturizers

E3-Rated • Fragrance Free • SKU 42334

Manufactured for

Georgia-Pacific Consumer Products. Atlanta, GA 30303-2529

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

or visit us online at www.gppro.com

©2020 GP PRO. All rights reserved.

alcohol permit SDS-NJ-20007

5000011192/000/00

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Foam Hand Sanitizer with Moisturizers

1000 mL (33.8 FL OZ)

NDC - 54622-423-01

FrontFrontRearRear

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
616805ethanol 70 % Topical FoamPSN1
616805ethanol 0.7 ML/ML Topical FoamSCD1
616805ethanol 70 % Topical FoamSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
54622-423-012024-01-30C16284748780-11030e365-1580-111a-e063-dadaa90a10e2enMotion Foam Sanitizer with Moisturizers, Fragrance Free

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
54622-423-01enMotion Foam Sanitizer with Moisturizers Fragrance Free1000 mL in 1 BOTTLE, DISPENSINGSOLUTION10001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
54622-423ENMOTION FOAM SANITIZER WITH MOISTURIZERS FRAGRANCE FREE (ETHYL ALCOHOL) SOLUTION [GEORGIA PACIFIC CONSUMER PRODUCTS]1Legacy NDC, 1 package rows20210601_6b578846-28f9-4dba-b7f6-8677fe9340ce.zip

Products#

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

DailyMed product names page 1 of 1 · 14 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
54622-42354622-423-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 12 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
bde4f682-e113-29f3-e053-2a95a90a0d9e6b578846-28f9-4dba-b7f6-8677fe9340ce2021-03-23WarningsExact identifier
spl id: bde4f682-e113-29f3-e053-2a95a90a0d9e
spl set id: 6b578846-28f9-4dba-b7f6-8677fe9340ce

Reported adverse events (FAERS/openFDA)#

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