ZEP FOAM SAN- benzalkonium chloride liquid

Zep Foam San by

Drug Labeling and Warnings

Zep Foam San 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

• Kills 99.99% of most common germs that cause illness in as little as 15 seconds.
• Sanitizing to decrease bacteria on skin.
• 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 using 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

• 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).
• Do not freeze.
• 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-I-BUY-ZEP (1-877-428-9937)

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

ZEP FOAM SAN 
benzalkonium chloride liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 66949-108
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
GLYCERIN (UNII: PDC6A3C0OX)
PEG/PPG-18/18 DIMETHICONE (UNII: 9H0AO7T794)
IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB)
HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)
WATER (UNII: 059QF0KO0R)
DMDM HYDANTOIN (UNII: BYR0546TOW)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 66949-108-04	3300 mL in 1 CASE; Type 0: Not a Combination Product	03/18/2003
2	NDC: 66949-108-09	6000 mL in 1 CASE; Type 0: Not a Combination Product	03/18/2003
3	NDC: 66949-108-85	208198 mL in 1 DRUM; Type 0: Not a Combination Product	03/18/2003

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	03/18/2003

Labeler - Zep Inc. (030471374)

Establishment
Name	Address	ID/FEI	Business Operations
Zep Inc.		112125310	manufacture(66949-108)