NEOSTRATA ANTIBACTERIAL FACIAL CLEANSER- triclosan liquid 
NeoStrata Company Inc

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.

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NeoStrata®
Antibacterial
Facial
Cleanser

Drug Facts

Active Ingredient

Triclosan 0.3%

Purpose

Antibacterial

Uses

Reduces potentially problematic bacteria on the skin

Warnings

For external use only

Do not apply to broken or inflamed skin.

When using this product keep out of eyes. Rinse with water to remove.

Stop use and ask a doctor if skin irritation develops and becomes severe.

Keep out of reach of children. If swallowed, get medical help or contact a poison control center right away.

Directions

  • Apply to wet skin and gently massage to develop foaming action
  • Rinse thoroughly with water
  • Use twice daily

Other Information

  • Store at 15°C-30°C (59°F-86°F)
  • You may report serious side effects to 1-800-628-9904

Inactive Ingredients

Ammonium Chloride, Ammonium Laureth Sulfate, Anthemis Noblis (Chamomile) Flower Extract, Aqua (Water), Cocamidopropyl Betaine, Disodium Cocoamphodiacetate, Gluconolactone, Glycine, Lauryl Alcohol, Methylparaben, Panthenol, PEG-80 Sorbitan Laurate, Phenoxyethanol, Polyquaternium-10, Propylene Glycol, Propylparaben, Sodium Chloride, Sodium Laureth Sulfate, Triethanolamine.

PRINCIPAL DISPLAY PANEL - 177ml Carton

NeoStrata®

REFINE

Antiaging for oily and
blemish prone skin

Antibacterial
Facial
Cleanser

4 PHA

6.0 fl oz / 177 ml e

Principal Display Panel - 177ml Carton
NEOSTRATA ANTIBACTERIAL FACIAL CLEANSER 
triclosan liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:58414-8321
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
TRICLOSAN (UNII: 4NM5039Y5X) (TRICLOSAN - UNII:4NM5039Y5X) TRICLOSAN3 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
AMMONIUM CHLORIDE (UNII: 01Q9PC255D)  
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)  
GLUCONOLACTONE (UNII: WQ29KQ9POT)  
GLYCINE (UNII: TE7660XO1C)  
LAURYL ALCOHOL (UNII: 178A96NLP2)  
METHYLPARABEN (UNII: A2I8C7HI9T)  
PANTHENOL (UNII: WV9CM0O67Z)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
PROPYLPARABEN (UNII: Z8IX2SC1OH)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM LAURETH-3 SULFATE (UNII: BPV390UAP0)  
TROLAMINE (UNII: 9O3K93S3TK)  
SULFATE ION (UNII: 7IS9N8KPMG)  
CHAMOMILE (UNII: FGL3685T2X)  
POLYQUATERNIUM-10 (400 MPA.S AT 2%) (UNII: HB1401PQFS)  
DISODIUM COCOAMPHODIACETATE (UNII: 18L9G3U51M)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:58414-8321-11 in 1 CARTON
1177 mL in 1 BOTTLE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC MONOGRAPH NOT FINALpart333E04/25/201111/12/2018
Labeler - NeoStrata Company Inc (605754829)

Revised: 2/2016
Document Id: e1238489-0b98-4cce-8f74-38bbc44bc19f
Set id: 0cc61f9f-2910-42c0-8b9a-9085dabcb05f
Version: 3
Effective Time: 20160219
 
NeoStrata Company Inc