Harbor Mist Alco-Foam Hand Sanitizer

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 Alco-Foam Hand Sanitizer
Active ingredientALCOHOL
Label structure8 sections

Indications and uses

For hand sanitizing to decrease bacteria on the skin that can cause disease. Recommended for repeated uses.

Dosage and administration

Place enough product in your palm to thoroughly cover your hands. Rub hands together briskly until dry. Children under 6 yearsof age should be supervised when using this product.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 62%v/v

Purpose

OTC - PURPOSE SECTION

Sanitizer

Uses:

INDICATIONS & USAGE SECTION

For hand sanitizing to decrease bacteria on the skin that can cause disease.

Recommended for repeated uses.

Warnings:

WARNINGS SECTION

Flammable. Keep away from fire or flame.

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 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

Place enough product in your palm to thoroughly cover your hands.

Rub hands together briskly until dry.

Children under 6 yearsof age should be supervised when using this product.

Other Information:

OTHER SAFETY INFORMATION

Store below 110 F (43 C).

May discolor certain fabrics or surfaces.

Inactive Ingredients:

INACTIVE INGREDIENT SECTION

Aqua, DEA-C8-C18 Perfluoroalkylethyl Phosphate

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Harbor

HARBOR MIST ALCO-FOAM

HAND SANITIZER

QUESTIONS?

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

1

PET

NSF

Nonfood Compounds

Program Listed (E3)

(Registration #164058)

Item #H740AS

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
616763ethanol 62 % Topical FoamPSN2
616763ethanol 0.62 ML/ML Topical FoamSCD2
616763ethanol 62 % Topical FoamSY2

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
81792-003-01Harbor Mist Alco-Foam Hand Sanitizer1250 mL in 1 BOTTLELIQUID12502

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
81792-003HARBOR MIST ALCO-FOAM HAND SANITIZER (ALCOHOL) LIQUID [VON DREHLE CORPORATION]2Current NDC, Legacy NDC, 1 package rows20241127_bfdefc20-494e-6156-e053-2995a90a77cb.zip

Products#

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

DailyMed product names page 1 of 1 · 4 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
81792-00381792-003-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 3 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 Alco-Foam Hand SanitizerALCOHOLVon Drehle Corporationbfdefc20-494e-6156-e053-2995a90a77cb2024-11-25WarningsExact identifier
ndc (package): 81792-003-01
ndc (product): 81792-003
ndc11 (package): 81792000301
spl id: 27c51ad3-5f7e-032d-e063-6394a90a4860
spl set id: bfdefc20-494e-6156-e053-2995a90a77cb

Reported adverse events (FAERS/openFDA)#

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