FINIPIL PRO/ELEC- benzethonium chloride cream

finipil pro/elec by

Drug Labeling and Warnings

finipil pro/elec by is a Otc medication manufactured, distributed, or labeled by Equibal, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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

INGREDIENTS AND APPEARANCE

FINIPIL PRO/ELEC  
benzethonium chloride cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 53228-001
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZETHONIUM CHLORIDE (UNII: PH41D05744) (BENZETHONIUM - UNII:1VU15B70BP)	BENZETHONIUM CHLORIDE	195 mg  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
BEHENTRIMONIUM METHOSULFATE (UNII: 5SHP745C61)
LEVOMENOL (UNII: 24WE03BX2T)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
CETYL ALCOHOL (UNII: 936JST6JCN)
CHLORHEXIDINE GLUCONATE (UNII: MOR84MUD8E)
DIMETHICONE (UNII: 92RU3N3Y1O)
MATRICARIA RECUTITA (UNII: G0R4UBI2ZZ)
MENTHYL LACTATE, (-)- (UNII: 2BF9E65L7I)
OCTYLDODECANOL (UNII: 461N1O614Y)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
POLYQUATERNIUM-37 (25000 MPA.S) (UNII: 31L31U8285)
STEARIC ACID (UNII: 4ELV7Z65AP)
WATER (UNII: 059QF0KO0R)
HAMAMELIS VIRGINIANA TOP (UNII: UDA30A2JJY)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 53228-001-01	75 mL in 1 TUBE; Type 0: Not a Combination Product	03/01/2013
2	NDC: 53228-001-02	3.6 mL in 1 PACKET; Type 0: Not a Combination Product	03/01/2013

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	03/01/2013

Labeler - Equibal, Inc. (144679883)

Registrant - Equibal, Inc. (144679883)

Establishment
Name	Address	ID/FEI	Business Operations
Equibal, Inc.		144679883	manufacture(53228-001)