Label: NU SKIN CLEAR ACTION ACNE MEDICATION DAY TREATMENT- salicylic acid gel

  • Category: HUMAN OTC DRUG LABEL

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Drug Label Information

Updated January 12, 2022

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  • 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.
    • Cover the entire face with a thin layer every morning after toner.
    • If bothersome dryness or peeling occurs, reduce application to every other day.
  • 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
  • INGREDIENTS AND APPEARANCE
    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)
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