DrugCite

ZEP FOAM SAN - benzethonium chloride liquid 
ZEP NON ALCOHOL FOAM SANITIZER - benzethonium chloride liquid 
Zep Inc.

Alcohol Free Foaming Hand Sanitizer

Active ingredient

Benzethonium chloride 0.2%

Purpose

Antiseptic

Uses

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

Warnings

For external use only.

When using this product

  • Avoid eye contact.
  • If in eyes, rinse promptly and thoroughly with water.

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

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

If swallowed, get medical help or contact a Poison Control Center immediately.

Directions

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

Other information

  • Store at 20 to 25C (68 to 77F).
  • 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 butylcarbomate, hydroxypropyl methylcellulose

Questions or comments?

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

0880.jpg


ZEP FOAM SAN 
benzethonium chloride  liquid
Product Information
Product Type HUMAN OTC DRUG NDC Product Code (Source) 66949-880
Route of Administration TOPICAL DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
BENZETHONIUM CHLORIDE (BENZETHONIUM) BENZETHONIUM CHLORIDE .02 g  in 10 mL
Inactive Ingredients
Ingredient Name Strength
WATER  
GLYCERIN  
PEG/PPG-18/18 DIMETHICONE  
DMDM HYDANTOIN  
IODOPROPYNYL BUTYLCARBAMATE  
HYDROXYPROPYL METHYLCELLULOSE E5 [II]  
Product Characteristics
Color      Score     
Shape Size
Flavor Imprint Code
Contains     
Packaging
# NDC Package Description Multilevel Packaging
1 66949-880-03 550 mL In 1 BOTTLE, PLASTIC None
2 66949-880-10 1000 mL In 1 BOTTLE, PLASTIC None
3 66949-880-12 2500 mL In 1 BOTTLE, PLASTIC None
4 66949-880-50 75708 mL In 1 PACKAGE None

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC monograph not final part333E 03/18/2003

ZEP NON ALCOHOL FOAM SANITIZER 
benzethonium chloride  liquid
Product Information
Product Type HUMAN OTC DRUG NDC Product Code (Source) 66949-248
Route of Administration TOPICAL DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
BENZETHONIUM CHLORIDE (BENZETHONIUM) BENZETHONIUM CHLORIDE .02 g  in 10 mL
Inactive Ingredients
Ingredient Name Strength
WATER  
GLYCERIN  
PEG/PPG-18/18 DIMETHICONE  
DMDM HYDANTOIN  
IODOPROPYNYL BUTYLCARBAMATE  
HYDROXYPROPYL METHYLCELLULOSE E5 [II]  
Product Characteristics
Color      Score     
Shape Size
Flavor Imprint Code
Contains     
Packaging
# NDC Package Description Multilevel Packaging
1 66949-248-15 550 mL In 1 BOTTLE, PLASTIC None

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC monograph not final part333E 07/14/2011

Labeler - Zep Inc. (030471374)
Establishment
Name Address ID/FEI Operations
Zep Inc. 030471374 manufacture
Revised: 12/2012Zep Inc.