Skip to Content

Fuzion AB Foam

Dosage form: liquid
Ingredients: BENZALKONIUM CHLORIDE 0.013g in 10mL
Labeler: Zep Inc.
NDC Code: 66949-388

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Fuzion AB Foam HS

Active ingredient

Purpose

Antibacterial Hand Wash

Uses

For washing to decrease bacteria on hands.

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 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.

Directions
  • Wet hands with water.
  • Press pump to dispense product into hands.
  • Massage soap into hands and wrists, emphasizing back of hands, knuckles and cuticles.
  • Rinse hands thoroughly and dry.
  • Store at 20 to 25°C (68 to 77°F).
  • Dispose in accordance with all applicable federal, state and local regulations.

Water; Cetrimonium Chloride, Lauryl/ Myristyl Amidopropyl Amine Oxide, Glycerin, Di-PPG-2 Myreth-10 Adipate, tetrasodium iminodisuccinate, Methylchloroisothiazolinone (and) Methylisothiazolinone, fragrance, Glutaral, citric acid; Red 4; Yellow 5

Questions or comments?

Call 1-877-I-BUY-ZEP

FUZION AB FOAM 
benzalkonium chloride liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:66949-388
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZALKONIUM CHLORIDE (BENZALKONIUM) BENZALKONIUM CHLORIDE0.013 g  in 10 mL
Inactive Ingredients
Ingredient NameStrength
FD&C RED NO. 4 
ANHYDROUS CITRIC ACID 
FD&C YELLOW NO. 5 
CETRIMONIUM CHLORIDE 
DI-PPG-2 MYRETH-10 ADIPATE 
METHYLCHLOROISOTHIAZOLINONE/METHYLISOTHIAZOLINONE MIXTURE 
GLUTARAL 
LAUROYL/MYRISTOYL AMIDOPROPYL AMINE OXIDE 
GLYCERIN 
TETRASODIUM IMINODISUCCINATE 
WATER 
Packaging
#Item CodePackage Description
1NDC:66949-388-161200 mL in 1 BOTTLE, PLASTIC
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A03/10/2017
Labeler - Zep Inc. (030471374)
Establishment
NameAddressID/FEIOperations
Zep Inc.030471374manufacture(66949-388)

Revised: 10/2017
 
Zep Inc.

Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate that the drug or combination is safe, effective or appropriate for any given patient. If you have questions about the substances you are taking, check with your doctor, nurse or pharmacist.

Hide