NU SKIN CLEAR ACTION  ACNE MEDICATION NIGHT TREATMENT- salicylic acid gel 
NSE Products, 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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Nu Skin Clear Action®
Acne Medication Night Treatment

Drug Facts

Active ingredient

Salicylic Acid (0.5%)

Purpose

Acne treatment

Use

Warnings

  • For external use only. Using other topical acne medication at the same time or immediately following the use of this product may increase dryness or irritation of the skin. If this occurs, only one medication should be used unless directed by a doctor.

  • Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

  • Cleanse the skin thoroughly before applying medication.
  • Cover the entire affected area with a thin layer once daily.
  • If bothersome dryness or peeling occurs, reduce application to every other day.

Inactive ingredients

Water (Aqua), Butylene Gylcol, Methyl Gluceth-20, Ethoxydiglycol, Polyacrylamide, Cyclodextrin/Retinol, Thioctic Acid,1 Tocopheryl Acetate, Camellia Sinensis Leaf Extract, Phytosphingosine, Glycyrrhiza Glabra (Licorice) Root Extract, Glycerin, Laureth-7, C13-14 Isoparaffin, BHT, Sodium Hydroxide, Tetrasodium EDTA, Fragrance (Parfum), Chlorphenesin, Methylparaben, Propylparaben.


1
Alpha Lipoic Acid.

Questions?

1-888-742-7626

PRINCIPAL DISPLAY PANEL - 30 ml Carton

Nu Skin Clear Action®

Acne Medication Night Treatment

NU SKIN®

30 ml e 1.0 fl. oz.

Principal Display Panel
NU SKIN CLEAR ACTION   ACNE MEDICATION NIGHT TREATMENT
salicylic acid gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:62839-0390
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Salicylic Acid (UNII: O414PZ4LPZ) (Salicylic Acid - UNII:O414PZ4LPZ) Salicylic Acid5 g  in 1000 mL
Inactive Ingredients
Ingredient NameStrength
Water (UNII: 059QF0KO0R)  
Butylene Glycol (UNII: 3XUS85K0RA)  
Methyl Gluceth-20 (UNII: J3QD0LD11P)  
Diethylene Glycol Monoethyl Ether (UNII: A1A1I8X02B)  
Alpha Lipoic Acid (UNII: 73Y7P0K73Y)  
Green Tea Leaf (UNII: W2ZU1RY8B0)  
Glycyrrhiza Glabra (UNII: 2788Z9758H)  
Glycerin (UNII: PDC6A3C0OX)  
Laureth-7 (UNII: Z95S6G8201)  
C13-14 Isoparaffin (UNII: E4F12ROE70)  
Butylated Hydroxytoluene (UNII: 1P9D0Z171K)  
Sodium Hydroxide (UNII: 55X04QC32I)  
Edetate Sodium (UNII: MP1J8420LU)  
Chlorphenesin (UNII: I670DAL4SZ)  
Methylparaben (UNII: A2I8C7HI9T)  
Propylparaben (UNII: Z8IX2SC1OH)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:62839-0390-11 in 1 CARTON
130 mL in 1 TUBE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC MONOGRAPH FINALpart333D09/01/2010
Labeler - NSE Products, Inc. (966817975)

Revised: 5/2011
Document Id: a0e5a958-f9a4-488b-bc19-eb591e299cfe
Set id: be125d02-b74a-49bd-90e6-2eac6f513923
Version: 1
Effective Time: 20110516
 
NSE Products, Inc.