DrugCite

MICROMOUSSE II ALCOHOL FREE HAND SANITIZING FOAM  - benzethonium chloride liquid 
United Laboratories, Inc.

MicroMousse II Alcohol-Free Hand Sanitizing Foam 6575 Drug Facts and Label

Drug Facts Box OTC-Active Ingredient Section

benzethonium chloride USP 0.2%

Drug Facts Box OTC-Indications & Usage Section

For hand-washing to decrease bacteria on the skin, only when water is not available

Drug Facts Box OTC-Warnings Section

For external use only

Drug Facts Box OTC-Purpose Section

Antiseptic

Drug Facts Box-OTC When Using Section

do not get into eyes

if contact occurs, rinse eyes thoroughly with water

Drug Facts Box-OTC Stop Use Section

irritation and redness develop

Drug Facts Box-OTC Keep Out Of Reach Of Children Section

If swallowed, get medical help or contact a Poison Control Center right away

Drug Facts Box-OTC Dosage & Administration Section

press pump twice to deliver two squirts (about a quarter size) of foaming product onto the palm of your hand

rub hands together until dry

wash hands with soap and water at earliest opportunity

Drug Facts Box-OTC Inactive Ingredient Section

water, glycerine, dimethicone, DMDM hydantoin, iodopropynl butylcarbamate, fragrance

MicroMousse II Alcohol-Free Hand Sanitizing Foam 6575 4 oz

6575Z8S85650.jpg  MicroMousse II Alcohol-Free Hand Sanitizing Foam 4 ozimage of bottle label


MICROMOUSSE II ALCOHOL FREE HAND SANITIZING FOAM 
benzethonium chloride  liquid
Product Information
Product Type HUMAN OTC DRUG NDC Product Code (Source) 63998-575
Route of Administration TOPICAL DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
BENZETHONIUM CHLORIDE (BENZETHONIUM) BENZETHONIUM CHLORIDE 2 mg  in 1 mL
Inactive Ingredients
Ingredient Name Strength
WATER  
GLYCERIN  
DIMETHICONE  
1,3-DIMETHYLOL-5,5-DIMETHYL-HYDANTOIN  
IODOPROPYNYL BUTYLCARBAMATE  
Product Characteristics
Color      Score     
Shape Size
Flavor Imprint Code
Contains     
Packaging
# NDC Package Description Multilevel Packaging
1 63998-575-10 1000 mL In 1 CARTRIDGE None
2 63998-575-12 1000 mL In 1 BAG None
3 63998-575-13 800 mL In 1 BAG None
4 63998-575-14 3785 mL In 1 BOTTLE, PLASTIC None
5 63998-575-15 946 mL In 1 BOTTLE, PLASTIC None
6 63998-575-16 236 mL In 1 BOTTLE, PLASTIC None
7 63998-575-17 532 mL In 1 BOTTLE, PLASTIC None
8 63998-575-18 50 mL In 1 BOTTLE, PLASTIC None
9 63998-575-24 115 mL In 1 BOTTLE, PLASTIC None
10 63998-575-55 208200 mL In 1 DRUM None

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC monograph not final part333 11/30/2009

Labeler - United Laboratories, Inc. (001759737)
Registrant - ABC Compounding Co., Inc. (003284353)
Establishment
Name Address ID/FEI Operations
ABC Compounding Co., Inc. 003284353 manufacture
Revised: 02/2010United Laboratories, Inc.