Harbor Mist E2 Sanitizing Foam with BZK

Manufacturer
Von Drehle Corporation | Woodbine Products Company
Effective date
2024-11-25
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 00:39:26

Label at a glance#

ProductHarbor Mist E2 Sanitizing Foam with BZK
Active ingredientBENZALKONIUM CHLORIDE
Label structure8 sections

Indications and uses

For hand washing to decrease bacteria on the skin. Recommended for repeated use.

Dosage and administration

Directions: Pump a small amount of foam into palm of hand. Rub thoroughly over all surfaces of both hands for 15 sec. Rinse with potable water.

Storage and handling

Store at 20 to 25 C (68-77 F)

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.13%

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Uses:

INDICATIONS & USAGE SECTION

For hand washing to decrease bacteria on the skin.

Recommended for repeated use.

Warnings:

WARNINGS SECTION

For external use only.

OTC - WHEN USING SECTION

When using this productavoid contact with eyes.

In case of eye contact, flush eyes with water.

OTC - STOP USE SECTION

Stop use and ask a doctorif irritation or redness develops, or if condition persists for more than 72 hours.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.

Directions:

DOSAGE & ADMINISTRATION SECTION

Directions:

Pump a small amount of foam into palm of hand.

Rub thoroughly over all surfaces of both hands for 15 sec.

Rinse with potable water.

Other Information:

STORAGE AND HANDLING SECTION

Store at 20 to 25 C (68-77 F)

Inactive ingredients:

INACTIVE INGREDIENT SECTION

Water, Coco-Glucoside, Lautrimonoium Chloride, Cocamidopropylamine Oxide, Citric Acid.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Harbor

HARBOR MIST E2 SANITIZING

FOAM SOAP WITH BZK

Manufactured for von Drehle Corporation I Hickory, NC 28601

QUESTIONS?

Call 800-438-3631 or visit us online at harbortowelandtissue.com.

NSF

Nonfood Compounds

Program listed (E2)

(Registration #000000)

1

PET

Item #H700E2

1250 ml (42 fl. oz.)

Made in the U.S.A.

container labelcontainer label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1046593benzalkonium chloride 0.13 % Medicated Liquid SoapPSN2
1046593benzalkonium chloride 1.3 MG/ML Medicated Liquid SoapSCD2
1046593benzalkonium chloride 0.13 % Medicated Liquid SoapSY2
1046593benzalkonium chloride 1.33 MG/ML Medicated Liquid SoapSY2

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
81792-004-01Harbor Mist E2 Sanitizing Foam with BZK1250 mL in 1 BOTTLELIQUID12502

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
81792-004HARBOR MIST E2 SANITIZING FOAM WITH BZK (BENZALKONIUM CHLORIDE) LIQUID [VON DREHLE CORPORATION]2Current NDC, Legacy NDC, 1 package rows20241127_c3b710b5-cf40-0e09-e053-2a95a90a2173.zip

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
81792-00481792-004-01

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
Harbor Mist E2 Sanitizing Foam with BZKBENZALKONIUM CHLORIDEVon Drehle Corporationc3b710b5-cf40-0e09-e053-2a95a90a21732024-11-25WarningsExact identifier
ndc (package): 81792-004-01
ndc (product): 81792-004
ndc11 (package): 81792000401
spl id: 27c5217b-8a15-7cbe-e063-6394a90a16ed
spl set id: c3b710b5-cf40-0e09-e053-2a95a90a2173

Reported adverse events (FAERS/openFDA)#

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