EXUVIANCE MOISTURIZING 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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Exuviance®
Moisturizing
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 - 212 ml Carton

Exuviance®

DERMATOLOGIST DEVELOPED

Moisturizing
Antibacterial
Facial Cleanser

  • Removes makeup, dirt,
    and excess oil
  • Fragrance-free

7.2 fl oz /212 ml

PRINCIPAL DISPLAY PANEL - 212 ml Carton
EXUVIANCE MOISTURIZING ANTIBACTERIAL FACIAL CLEANSER 
triclosan liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:58414-8748
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
AMMONIUM CHLORIDE (UNII: 01Q9PC255D)  
WATER (UNII: 059QF0KO0R)  
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:58414-8748-11 in 1 CARTON
1212 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: 83a570bb-28a5-4049-8930-643c865ad9f1
Set id: fca587ab-73a3-4c9b-b5a3-cd51f93b2289
Version: 3
Effective Time: 20160219
 
NeoStrata Company Inc