ZEP E-2 FOAMING SANITIZING HAND CLEANER- chloroxylenol liquid

Zep E-2 Foaming Sanitizing Hand Cleaner by

Drug Labeling and Warnings

Zep E-2 Foaming Sanitizing 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

Chloroxylenol 3.0%

Purpose

Antiseptic Hand Wash

Uses

Hand sanitizing to decrease bacteria on the skin.

Warnings

For external use only. Do not usein or around the eyes; if in eyes, rinse promptly and thoroughly with water.

When using this product

• Avoid eye contact.
• If in the eyes, rinse promptly and throoughly with water. Do not swallow.
• If swallowed, do not induce vomiting and if individual is conscious, give large quantities of water to dring and consult a physician immediately.
• Allergy Alert: May cause skin reactions. Symptoms may include: skin reddening, blisters and rash. If a skin reaction occurs, stop use and seek medical help right away.

STOP USE

Stop use and ask a doctor if skin irritation or redness persists for more than 72 hours.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children and pets. Children must be supervised in use of this product.

ASK DOCTOR

If swallowed, get medical help or contact a Poison Control center immediately.

Directions

• We hands with water.
• Apply liquid Soap.
• Massage soap into hands and wrists, emphasizing back of hands, knuckles and cuticles.
• Rinse hands thoroughly and dry.

Other information

• Store at 20 to 25°C (68 to 77°F).
• Dispose in accordance with all applicable federal, local and state regulations.

Inactive ingredients

Water, Sodium C14-16 Olefin Sulfonate, Triethylene Glycol, Cocamidopropyl Betain, Sodium Xylenesulfonate, PEG-75 Lanolin, Citric Acid

Questions or comments?

Call 1-800-I-BUY-ZEP (1-800-428-9937)

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

ZEP E-2 FOAMING SANITIZING HAND CLEANER 
chloroxylenol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 66949-994
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CHLOROXYLENOL (UNII: 0F32U78V2Q) (CHLOROXYLENOL - UNII:0F32U78V2Q)	CHLOROXYLENOL	3 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
SODIUM C14-16 OLEFIN SULFONATE (UNII: O9W3D3YF5U)
TRIETHYLENE GLYCOL (UNII: 3P5SU53360)
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
SODIUM XYLENESULFONATE (UNII: G4LZF950UR)
PEG-75 LANOLIN (UNII: 09179OX7TB)
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 66949-994-16	2500 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	06/19/2000

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	06/19/2000

Labeler - Zep Inc. (030471374)

Establishment
Name	Address	ID/FEI	Business Operations
Zep Inc.		112125310	manufacture(66949-994)