Pacific Blue Ultra Foaming

Manufacturer
Georgia-Pacific Consumer Products LP
Effective date
2025-01-23
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-06-01 00:53:29

Label at a glance#

ProductPacific Blue Ultra Foaming 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 and flame
  • For external use only

OTC - WHEN USING SECTION

When using this productdo not use in or near eyes.

OTC - STOP USE SECTION

Stop use and ask a doctorif irritation or redness develops.

If condition persists for more than 72 hours consult a doctor.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

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, Caprylic/Capric Triglyceride, Isopropyl Myristate

Additional rear label text

SPL UNCLASSIFIED SECTION

Pacific Blue Ultra

Foam Hand Sanitizer

Fragrance Free SKU 43335

Manufactured for

Georgia-Pacific Consumer Products. Atlanta, GA 30303

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

or visit us online at www.gppro.com

(c) 2019 GP PRO. All rights reserved.

alcohol permit SDS-KY-15002

43335-B2 PRD Rev A

principal display panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Foam Hand Sanitizer

1000 mL (33.8 FL OZ)

container labelcontainer label

container labelPBbcontainer labelPBb

container labelPBAbcontainer labelPBAb

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
616805ethanol 70 % Topical FoamPSN4
616805ethanol 0.7 ML/ML Topical FoamSCD4
616805ethanol 70 % Topical FoamSY4

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
54622-122-01Pacific Blue Ultra FoamingFragrance Free1000 mL in 1 BOTTLE, DISPENSINGSOLUTION10004

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
54622-122PACIFIC BLUE ULTRA FOAMING FRAGRANCE FREE (ETHYL ALCOHOL) SOLUTION [GEORGIA-PACIFIC CONSUMER PRODUCTS LP]4Current NDC, Legacy NDC, 1 package rows20250124_c4840ac2-978c-3aac-e053-2995a90ad312.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
54622-12254622-122-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 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
Pacific Blue Ultra Foaming Fragrance FreeETHYL ALCOHOLGeorgia-Pacific Consumer Products LPc4840ac2-978c-3aac-e053-2995a90ad3122025-01-23WarningsExact identifier
ndc (package): 54622-122-01
ndc (product): 54622-122
ndc11 (package): 54622012201
spl id: 2c631dee-f120-58af-e063-6394a90ac821
spl set id: c4840ac2-978c-3aac-e053-2995a90ad312

Reported adverse events (FAERS/openFDA)#

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