ALCOHOL FREE HAND SANITIZER- benzalkonium chloride aerosol, foam

Alcohol free hand sanitizer by

Drug Labeling and Warnings

Alcohol free hand sanitizer by is a Otc medication manufactured, distributed, or labeled by Sanihealth Products Corporation. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

DOSAGE & ADMINISTRATION

Directions

Place a palmful (5 grams) in one hand. Spread onto both hands to wrist and rub into the skin until dry.

INACTIVE INGREDIENT

Water (Aqua), Decyl Glucoside, Glycerin, Fragrance, DMDM Hydantoin

BOXED WARNING

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Warnings:

For external use only.

Keep out of reach of children.

Avoid eye contact. Should contact occur, rinse thoroughly with water.

If swallowed or irritation develops, discontinue use and consult a health care practitioner.

INDICATIONS & USAGE

Use

Use as part of your daily cleansing routine when soap and water are not available, or to supplement hand washing.

ACTIVE INGREDIENT

Active Ingredient                     Purpose

Benzalkonium Chloride 0.12%   Antiseptic

PRINCIPAL DISPLAY PANEL

Mission Linen supply

Mission linen and uniform service

Alcohol free hand sanitizer

benzalkonium chloride 0.12%

High performance alcohol free foam hand sanitizer

1 L (33.8 U.S. OZ)

INGREDIENTS AND APPEARANCE

ALCOHOL FREE HAND SANITIZER 
benzalkonium chloride aerosol, foam

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 51053-500
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	1.2 mL  in 1000 mL

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 51053-500-10	1000 mL in 1 BOTTLE, PUMP

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part352	05/24/2010

Labeler - Sanihealth Products Corporation (244200478)