NU SKIN CLEAR ACTION ACNE MEDICATION DAY 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 Day Treatment

Drug Facts

Active Ingredient

Salicylic Acid (0.5%)

Purpose

Acne treatment

Use

Warnings

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

Inactive Ingredients

Water (Aqua), Butylene Glycol, Methyl Pyrrolidone, Gluconolactone, Mandelic Acid, Sodium Hydroxide, Camellia Sinensis Leaf Extract,1 Glycerin, Sclerotium Gum, Arginine, Polyquaternium-10, Ethylene/Acrylic Acid Copolymer, Disodium EDTA, Chlorphenesin, Methylparaben.


1
White Tea

Questions?

1-888-742-7626

PRINCIPAL DISPLAY PANEL - 30 ml Carton

Nu Skin Clear Action®

Acne Medication Day Treatment

NU SKIN ®

30 ml e (1.0 fl. oz.)

Principal Display Panel - 30 ml Carton
NU SKIN  CLEAR ACTION ACNE MEDICATION DAY TREATMENT
salicylic acid gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:62839-1038
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)  
METHYLPYRROLIDONE (UNII: JR9CE63FPM)  
Gluconolactone (UNII: WQ29KQ9POT)  
Mandelic Acid (UNII: NH496X0UJX)  
Sodium Hydroxide (UNII: 55X04QC32I)  
Green Tea Leaf (UNII: W2ZU1RY8B0)  
Glycerin (UNII: PDC6A3C0OX)  
Arginine (UNII: 94ZLA3W45F)  
Edetate Disodium (UNII: 7FLD91C86K)  
Chlorphenesin (UNII: I670DAL4SZ)  
Methylparaben (UNII: A2I8C7HI9T)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:62839-1038-91 in 1 CARTON01/25/2002
130 mL in 1 TUBE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC MONOGRAPH FINALpart333D01/25/2002
Labeler - NSE Products, Inc. (803486393)

Revised: 1/2022
Document Id: d2cf983a-61aa-4305-83fb-1a2f3c90ef17
Set id: 92dbcb03-29a8-4cde-97e3-d81cc4ce8999
Version: 3
Effective Time: 20220112
 
NSE Products, Inc.