ZEP FS ANTIMICROBIAL FOAMING HAND CLEANER- benzalkonium chloride liquid

Zep FS Antimicrobial Foaming Hand Cleaner by

Drug Labeling and Warnings

Zep FS Antimicrobial Foaming 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 Hand Wash

Uses

• Hand washing to decrease bacteria on the skin.
• For use in food processing facilities.

Warnings

For external use only.

DO NOT USE

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

STOP USE

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

WHEN USING

• 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.

KEEP OUT OF REACH OF CHILDREN

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 writsts, emphasizing back of hands, knuckles and cuticles.
• Rise hands thoroughly and dry.

Other information

• Store at 20 to 25°C (68 to 77°F).
• Do not freeze.
• Dispose in accordance with all applicable federal, state and local regulations.

Inactive ingredients

Water, Cocamidopropyl Hydroxysultaine, Lauramine Oxide, Didecyldimonium Chloride, PEG-6 Cocamide, Phenoxyethanol, Iodopropynyl Butylcarbamate, Methylisothiazolinone, Hexanediol

Questions or comments?

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

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

ZEP FS ANTIMICROBIAL FOAMING HAND CLEANER 
benzalkonium chloride liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 66949-996
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
HEXANEDIOL (UNII: ZIA319275I)
WATER (UNII: 059QF0KO0R)
COCAMIDOPROPYL HYDROXYSULTAINE (UNII: 62V75NI93W)
LAURAMINE OXIDE (UNII: 4F6FC4MI8W)
PEG-6 COCAMIDE (UNII: YZ6NLA4O1E)
DIDECYLDIMONIUM CHLORIDE (UNII: JXN40O9Y9B)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB)
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 66949-996-11	6000 mL in 1 CASE; Type 0: Not a Combination Product	04/12/2006
2	NDC: 66949-996-16	10000 mL in 1 CASE; Type 0: Not a Combination Product	04/12/2006
3	NDC: 66949-996-85	208198 mL in 1 DRUM; Type 0: Not a Combination Product	04/12/2006
4	NDC: 66949-996-17	1200 mL in 1 CASE; Type 0: Not a Combination Product	04/12/2006

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	04/12/2006

Labeler - Zep Inc. (030471374)

Establishment
Name	Address	ID/FEI	Business Operations
Zep Inc.		112125310	manufacture(66949-996)