SafeHaven Personal Gel Hand Sanitizer

Manufacturer
Georgia-Pacific Consumer Products LP
Effective date
2023-12-15
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 21:18:07

Label at a glance#

ProductSafeHaven Personal Gel Hand Sanitizer
Active ingredientALCOHOL
Label structure7 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 71.9% 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 doctor if 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 (Aqua), Glycerin, Acrylates/C10-30 Alkyl Acrylates Crosspolymer, Glycereth-2 Cocoate, Triethanolamine

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

SafeHaven

Personal Gel Hand Sanitizer

Dye and Fragrance Free

20 - 1.25 FL OZ (36.9 mL)

Total: 25 FL OZ (738 mL)

Manufactured for

GP GeorgiaPacific

Georgia-Pacific Consumer Products

Atlanta, Georgia 30303-2529

Made in USA with foreign and domestic materials

(c) 2020 GP PRO.

All rights reserved.

Unless otherwise noted, all trademarks are owned by or licensed to Georgia-Pacific Consumer Products.

Contact Geogia-Pacific at 1-866-HELLOGP(1-866-435-5647)

or visit: www,gppro.com

Alcohol Permit SDS-KY-15002

www.gppro.com

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Products#

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
54622-12954622-129-20

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 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
2c6331dd-f9bb-8726-e063-6394a90a8648c2b6776d-b7ce-c937-e053-2a95a90a26102025-01-23WarningsExact identifier
spl set id: c2b6776d-b7ce-c937-e053-2a95a90a2610

Reported adverse events (FAERS/openFDA)#

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