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finipil pro/elec

Medically reviewed on Dec 27, 2017

Dosage form: cream
Ingredients: BENZETHONIUM CHLORIDE 195mg in 100mL
Labeler: Equibal, Inc.
NDC Code: 53228-001

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.

Active Ingredient

DRUG FACTS

Active Ingredient

Benzethonium Chloride 0.2% w/w

Purpose

Purpose

Antiseptic


Keep out of reach of children.

Keep out of reach of children

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

Use(s)

Use(s)

  • first aid to help prevent bacterial contamination in minor cuts, scrapes and burns.
  • cools, soothes and moisturizes after hair removal.
  • use immediately after hair removal

Warnings Do not use in conjunction

Warnings

For external use only

Do not use in conjunction

with products containing acids

Ask a doctor if

Ask a doctor if pregnant or breast feeding,

Stop use and ask a doctor if

Stop use and ask a doctor if

irritation and redness develop

Directions

Directions

Apply a small amount after Nufree®  or electric hair removal

When using this product

When using this product do not get into eyes.

If contact occurs, rinse eyes thoroughly with water.

Inactive ingredients

Inactive ingredients

Behentrimonium Methosulfate, Bisabolol, Butylene Glycol, Cetyl Alcohol, Chlorhexidine Gluconate, Dimethicone, Matricaria (Chamomile Recutita) Extract, Menthyl Lactate, Octyldodecanol, Phenoxyethanol, Polyquarternium-37, Stearic Acid, Water, Witch Hazel (Hamamelis Virginiana) Extract 

Product Label

finipil ®

patented

pro/elec

ANTISEPTIC CREAM

for professional use only

Protects against infection

Soothes and moisturizes skin

noncomedogenic

2.5 fl oz 75 ml

equibal labs

800-247-2405

www.nufree.com

Made in U.S.A.

not tested on animals

patent # 7,078,050



FINIPIL PRO/ELEC  
benzethonium chloride cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:53228-001
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZETHONIUM CHLORIDE (BENZETHONIUM) BENZETHONIUM CHLORIDE195 mg  in 100 mL
Inactive Ingredients
Ingredient NameStrength
BEHENTRIMONIUM METHOSULFATE 
LEVOMENOL 
BUTYLENE GLYCOL 
CETYL ALCOHOL 
CHLORHEXIDINE GLUCONATE 
DIMETHICONE 
MATRICARIA RECUTITA 
MENTHYL LACTATE, (-)- 
OCTYLDODECANOL 
PHENOXYETHANOL 
POLYQUATERNIUM-37 (25000 MPA.S) 
STEARIC ACID 
WATER 
HAMAMELIS VIRGINIANA TOP 
Packaging
#Item CodePackage Description
1NDC:53228-001-0175 mL in 1 TUBE
2NDC:53228-001-023.6 mL in 1 PACKET
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A03/01/2013
Labeler - Equibal, Inc. (144679883)
Registrant - Equibal, Inc. (144679883)
Establishment
NameAddressID/FEIOperations
Equibal, Inc.144679883manufacture(53228-001)

 
Equibal, Inc.

Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.

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