HY5 ALCOHOL FREE FRAGRANCE FREE FOAMING HAND SANITIZER- benzalkonium chloride liquid

Hy5 Alcohol Free Fragrance Free Foaming Hand Sanitizer by

Drug Labeling and Warnings

Hy5 Alcohol Free Fragrance Free Foaming Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Deb USA, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active ingredient

Benzalkonium Chloride 0.13%

PURPOSE

Purpose

Antibacterial

INDICATIONS & USAGE

Uses

For hand sanitizing to reduce bacteria on the skin

WARNINGS

Warnings

For external use only

When using this product avoid contact with eyes.  In case of eye contact, flush with water.

Keep out of reach of children.  If swallowed, get medical help or contact a Poison Control Center right away.

DOSAGE & ADMINISTRATION

Directions

Apply one shot to dry hands, rub into skin

No rinsing required

INACTIVE INGREDIENT

Inactive ingredients

Water, Propylene Glycol, Aloe Barbadensis Leaf Juice, Cocamidopropyl Betaine, Lauramine Oxide, Tetrasodium EDTA, Magnesium Nitrate, Methylchloroisothiazolinone, Magnesium Chloride, Methylisothiazolinone

PRINCIPAL DISPLAY PANEL

Hy5 Alcohol Free Hand Sanitizer

Alcohol Free Fragrance Free Foaming Hand Sanitizer

55833

Manufactured for

DermaCare, Inc.

P.O. Box 25263, Sarasota, FL  34277

Ph:  1-877-hy5-5678

www.hy5sanitizer.com

1200 mL 40.6 Fluid Ounces

Rev. 08-11

INGREDIENTS AND APPEARANCE

HY5 ALCOHOL FREE FRAGRANCE FREE FOAMING HAND SANITIZER 
benzalkonium chloride liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 11084-138
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.13 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
LAURAMINE OXIDE (UNII: 4F6FC4MI8W)
EDETATE SODIUM (UNII: MP1J8420LU)
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
MAGNESIUM NITRATE (UNII: 77CBG3UN78)
MAGNESIUM CHLORIDE (UNII: 02F3473H9O)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 11084-138-12	1200 mL in 1 BOTTLE, PLASTIC

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	08/15/2011

Labeler - Deb USA, Inc. (607378015)

Establishment
Name	Address	ID/FEI	Business Operations
Deb USA, Inc.		607378015	manufacture