ZEP E-2 HAND SANITIZING CLEANER- chloroxylenol liquid

Zep E-2 Hand Sanitizing Cleaner by

Drug Labeling and Warnings

Zep E-2 Hand Sanitizing 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 washing to decrease bacteria on skin

Warnings

For external use only.

DO NOT USE

Do not use in or around the eyes.

WHEN USING

When using this product

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

Stop use and ask a doctor

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

Keep out of reach of children and pets.

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

Directions

• Wet hands with water.
• Place hands under dispenser and 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 room temperature.
• Do not freeze.
• Dispose in accordance with all applicable federal, state and local regulations.

Inactive ingredients

Water, Sodium C14-16 Olefin Sulfonate, Triethylene Glycol, Cocamidopropyl Hydroxysultaine, Hydroxyethyl Cellulose, PEG-75 Lanolin, Methylchloroisothiazolinone, Methylisothiazolinone, Citric Acid

Questions of comments?

Call 1-877-I-BUY_ZEP (1-877-428-9937)

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

ZEP E-2 HAND SANITIZING CLEANER 
chloroxylenol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 66949-920
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 HYDROXYSULTAINE (UNII: 62V75NI93W)
HYDROXYETHYL CELLULOSE (2000 CPS AT 1%) (UNII: S38J6RZN16)
PEG-75 LANOLIN (UNII: 09179OX7TB)
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 66949-920-24	3785 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	06/15/1988
2	NDC: 66949-920-01	1000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	06/15/1988
3	NDC: 66949-920-06	6000 mL in 1 CASE; Type 0: Not a Combination Product	06/15/1988
4	NDC: 66949-920-85	208198 mL in 1 DRUM; Type 0: Not a Combination Product	06/15/1988

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	06/15/1988

Labeler - Zep Inc. (030471374)

Establishment
Name	Address	ID/FEI	Business Operations
Zep Inc.		112125310	manufacture(66949-920)