ZEP NON ALCOHOL FOAM SANITIZER- benzalkonium chloride liquid

Zep Non Alcohol Foam Sanitizer by

Drug Labeling and Warnings

Zep Non Alcohol Foam Sanitizer 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 Hand Wash

Uses

• Hand sanitizing to decrease bacteria on skin.
• Kills 99.99% of most common germs that cause illness in as little as 15 seconds.
• No rinsing required.
• Does not contain alcohol.

Warnings

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

When using this product

• 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.

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

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

Directions

• Press pump to dispense product onto hands.
• Rub hands together allowing foam to contact all areas, especially around the nails.
• Continue until foam has disappeared and/or hands are dry.

Other information

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

Inactive ingredients

Water, Glycerin, PEG/PPG-18/18 Dimethicone, DMDM Hydantoin and Iodopropynyl Butylcarbamate, Hydroxypropyl Methylcellulose

Questions or comments?

Call 1-877-BUY-ZEP (1-877-428-9937)

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

ZEP NON ALCOHOL FOAM SANITIZER 
benzalkonium chloride liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 66949-107
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 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)
WATER (UNII: 059QF0KO0R)
DMDM HYDANTOIN (UNII: BYR0546TOW)
GLYCERIN (UNII: PDC6A3C0OX)
IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB)
PEG/PPG-18/18 DIMETHICONE (UNII: 9H0AO7T794)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 66949-107-16	4800 mL in 1 CASE; Type 0: Not a Combination Product	07/14/2011

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	07/14/2011

Labeler - Zep Inc. (030471374)

Establishment
Name	Address	ID/FEI	Business Operations
Zep Inc.		112125310	manufacture(66949-107)