ZEP PROFESSIONAL E-2 HAND CLEANER- benzalkonium chloride liquid

Zep Professional E-2 Hand Cleaner by

Drug Labeling and Warnings

Zep Professional E-2 Hand Cleaner by is a Otc medication manufactured, distributed, or labeled by Zep Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Benzalkonium chloride 0.13%

Purpose

Antiseptic Handwash

Uses

• Hand sanitizing to decrease bacteria on skin
• For use in food processing facilities

Warnings

For external use only.

DO NOT USE

Can cause eye irritation. Avoid contact with eyes.

WHEN USING

When using this product

• Do not use in or around eyes. If eye contact occurs, rinse well with water for at least 15 minutes. Consult a physician.
• Do no swallow this product. If swallowed, do not induce vomiting. If individual is conscious, give large quantities of water to drink and consult a physician immediately.

STOP USE

Discontinue use if irritation and redness develops. If condition persists for more than 72 hours, consult a doctor.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children.

Directions

• Wet hands with water
• Dispense one or two squirts in palm of hand
• Massag soap into hands and wrists, emphasizing back of hands, knuckles and cuticles
• Hands must be thoroughly rinsed with potable water

Other information

• Keep container closed
• Store at room temperature
• Do not freeze
• Do not reuse empty container
• Dispose in accordance with all applicable federal, state & local regulations

Inactive ingredients

Water, Cocamidopropyl Betaine, Didecyldimethylammonium Chloride, PEG-6 Cocamide, Ethanol, Hydroxyethylcellusolose, DMDM Hydantoin (and) Iodopropynyl Butylcarbamate, Citric Acid

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

ZEP PROFESSIONAL E-2 HAND CLEANER 
benzalkonium chloride liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 66949-112
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	.013 g  in 10 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
DIDECYLDIMETHYLAMMONIUM CHLORIDE (UNII: JXN40O9Y9B)
PEG-6 COCAMIDE (UNII: YZ6NLA4O1E)
ALCOHOL (UNII: 3K9958V90M)
HYDROXYETHYL CELLULOSE (2000 CPS AT 1%) (UNII: S38J6RZN16)
DMDM HYDANTOIN (UNII: BYR0546TOW)
IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB)
GLUTARAL (UNII: T3C89M417N)
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 66949-112-01	1000 mL in 1 BOTTLE, PLASTIC
2	NDC: 66949-112-24	3785 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	04/07/2009

Labeler - Zep Inc. (030471374)

Establishment
Name	Address	ID/FEI	Business Operations
Zep Inc.		030471374	manufacture(66949-112)