ZEP FS ANTIMICROBIAL HAND CLEANER- benzalkonium chloride liquid FUZION ANTIMICROBIAL HAND CLEANER- benzalkonium chloride liquid

Fuzion Antimicrobial Hand Cleaner by

Drug Labeling and Warnings

Fuzion Antimicrobial 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 skin
• For use in food processing facilities

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 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 20 to 25 ºC (68 to 77 ºF).
• Do not freeze
• Dispose in accordance with all applicable federal, state & local regulations

Inactive ingredients

Water, Didecyldimethylammonium Chloride, Cocamidopropyl Hydroxysultaine, Lauramine Oxide, PEG-6 Cocamide, Hydroxyethylcellusolose, Phenoxyethanol, Iodopropynyl Butylcarbamate, Methylisothiazolinone, Hexanediol, Citric Acid, Sodium Citrate

Questions or comments?

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

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

ZEP FS ANTIMICROBIAL HAND CLEANER 
benzalkonium chloride liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 66949-901
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
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
HEXANEDIOL (UNII: ZIA319275I)
WATER (UNII: 059QF0KO0R)
COCAMIDOPROPYL HYDROXYSULTAINE (UNII: 62V75NI93W)
DIDECYLDIMONIUM CHLORIDE (UNII: JXN40O9Y9B)
LAURAMINE OXIDE (UNII: 4F6FC4MI8W)
HYDROXYETHYL CELLULOSE (2000 CPS AT 1%) (UNII: S38J6RZN16)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB)
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
PEG-6 COCAMIDE (UNII: YZ6NLA4O1E)
SODIUM CITRATE (UNII: 1Q73Q2JULR)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 66949-901-11	6000 mL in 1 CASE; Type 0: Not a Combination Product	02/26/1993
2	NDC: 66949-901-01	946.53 mL in 1 BOTTLE; Type 0: Not a Combination Product	02/26/1993
3	NDC: 66949-901-24	15140 mL in 1 CASE; Type 0: Not a Combination Product	02/26/1993
4	NDC: 66949-901-85	208198 mL in 1 DRUM; Type 0: Not a Combination Product	02/26/1993

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	02/26/1993

FUZION ANTIMICROBIAL HAND CLEANER 
benzalkonium chloride liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 66949-338
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
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
HEXANEDIOL (UNII: ZIA319275I)
DIDECYLDIMONIUM CHLORIDE (UNII: JXN40O9Y9B)
COCAMIDOPROPYL HYDROXYSULTAINE (UNII: 62V75NI93W)
LAURAMINE OXIDE (UNII: 4F6FC4MI8W)
IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB)
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
WATER (UNII: 059QF0KO0R)
HYDROXYETHYL CELLULOSE (2000 CPS AT 1%) (UNII: S38J6RZN16)
PEG-6 COCAMIDE (UNII: YZ6NLA4O1E)
SODIUM CITRATE (UNII: 1Q73Q2JULR)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 66949-338-16	4800 mL in 1 CASE; Type 0: Not a Combination Product	12/08/2015

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	12/08/2015

Labeler - Zep Inc. (030471374)

Establishment
Name	Address	ID/FEI	Business Operations
Zep Inc.		112125310	manufacture(66949-338, 66949-901)