FDA.reportPublic FDA data

enMotion Foam

Manufacturer
Georgia Pacific Consumer Products | Consumer Product Partners, LLC
Effective date
2024-10-22
Label type
HUMAN OTC DRUG LABEL
Version
12
Source
legacy-cache
Hydrated at
2026-08-01 20:51:37

Label at a glance#

ProductenMotion Foam
Active ingredientBENZALKONIUM CHLORIDE
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

Benzalkonium Chloride 0.1%w/w

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

For external use only

When using this product

OTC - WHEN USING SECTION

do not use in or near eyes.

Discontinue use

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, Decyl Glycoside, PEG-12 Dimethicone, Glycerin, Dipotassium Phosphate, Potassium Phosphate

SPL UNCLASSIFIED SECTION

PACIFIC BLUE ULTRA

Foam Hand Sanitizer

Alcohol Free

Fragrance Free SKU 43338

Manufactured for

Georgia-Pacific Consumer Products LP.  Atlanta, GA 30303

Questions? Call 1-866 HELLOGP (435-5647

or visit us on line at www.gppro.com

2017 Georgia-pacific Consumer Products LP. All rights reserved

43338-V1PRDRevA

146.000/146AA

principal display panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Foam Hand Sanitizer

Alcohol Free

1000 mL (33.8 FL OZ)

4333B-V2PRDRevA17

image descriptionimage description

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
54622-146ENMOTION FOAM (BENZALKONIUM CHLORIDE) SOLUTION [GEORGIA PACIFIC CONSUMER PRODUCTS]12Legacy NDC20241024_fb67f738-3523-4908-9e22-b247e63eee46.zip

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
54622-14654622-146-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
DECYL GLUCOSIDEZ17H97EA6YIACT
PEG-12 DIMETHICONEZEL54N6W95IACT
GLYCERINPDC6A3C0OXIACT
DIBASIC POTASSIUM PHOSPHATECI71S98N1ZIACT
POTASSIUM PHOSPHATE, MONOBASIC4J9FJ0HL51IACT
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB

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
3dfbe75e-990b-18d7-e063-6294a90ac32efb67f738-3523-4908-9e22-b247e63eee462025-09-04WarningsExact identifier
spl set id: fb67f738-3523-4908-9e22-b247e63eee46

Reported adverse events (FAERS/openFDA)#

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