Label: NU SKIN CLEAR ACTION- salicylic acid gel

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph final

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.

Drug Label Information

Updated May 16, 2011

If you are a consumer or patient please visit this version.

View All Sections
  • SPL UNCLASSIFIED SECTION

    Drug Facts

  • Active ingredient

    Salicylic Acid (0.5%)

  • Purpose

    Acne treatment

  • Use

    • For the treatment of acne.
    • Penetrates pores to eliminate most acne blemishes.
  • 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
  • INGREDIENTS AND APPEARANCE
    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)
View All Sections

Find additional resources

(also available in the left menu)

Safety

Report Adverse Events, FDA Safety Recalls, Presence in Breast Milk

Related Resources

Medline Plus, Clinical Trials, PubMed, Biochemical Data Summary

More Info on this Drug

View Labeling Archives, RxNorm, Get Label RSS Feed, View NDC Code(s)NEW!