HARBOR MIST ALCO-FOAM HAND SANITIZER- alcohol liquid

Harbor Mist Alco-Foam Hand Sanitizer by

Drug Labeling and Warnings

Harbor Mist Alco-Foam Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Von Drehle Corporation, Woodbine Products Company. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Ethyl Alcohol 62%v/v

Purpose

Sanitizer

Uses:

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

Recommended for repeated uses.

Warnings:

Flammable. Keep away from fire or flame.

For external use only.

When using this productavoid contact with eyes.

In case of eye contact, flush eyes with water.

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

Keep out of reach of children.

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

Directions:

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:

Store below 110 F (43 C).

May discolor certain fabrics or surfaces.

Inactive Ingredients:

Aqua, DEA-C8-C18 Perfluoroalkylethyl Phosphate

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.

INGREDIENTS AND APPEARANCE

HARBOR MIST ALCO-FOAM HAND SANITIZER 
alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 81792-003
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	62 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
DIETHANOLAMINE BIS(C8-C18 PERFLUOROALKYLETHYL)PHOSPHATE (UNII: 4J55VM509S)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 81792-003-01	1250 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/30/2021

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	04/30/2021

Labeler - Von Drehle Corporation (071054415)

Establishment
Name	Address	ID/FEI	Business Operations
Woodbine Products Company		004220323	manufacture(81792-003)