Label: NU SKIN CLEAR ACTION ACNE MEDICATION TONER- salicylic acid liquid

  • 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 January 12, 2022

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  • SPL UNCLASSIFIED SECTION

    Drug Facts

  • Active Ingredient

    Salicylic Acid (0.5%)

  • Purpose

    Acne treatment

  • Uses

    • For the treatment of acne.
    • Penetrates pores to eliminate most acne blemishes.
  • Warnings

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

    • 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.
  • Directions

    • Cleanse the skin thoroughly before applying medication.
    • To unlock, hold collar while turning pump counterclockwise.
    • Cover the entire affected area with a thin layer twice daily.
    • If bothersome dryness or peeling occurs, reduce application to once a day or every other day.
  • Inactive Ingredients

    Water (Aqua), Butylene Glycol, Betaine, Glycereth-26, Methyl Gluceth-20, PPG-5-Ceteth-20, Dipotassium Glycyrrhizate, Glycerin, Zinc PCA, Potassium Ascorbyl Tocopheryl Phosphate, Phenoxyethanol, Chlorphenesin, Phenethyl Alcohol, Methylparaben, Benzoic Acid.

  • Questions?

    1-888-742-7626

  • PRINCIPAL DISPLAY PANEL - 150 ml Bottle Label

    Nu Skin Clear Action®

    Acne Medication Toner

    NU SKIN®

    150 ml e (5 fl. oz.)

    Principal Display Panel - 150 ml Bottle Label
  • INGREDIENTS AND APPEARANCE
    NU SKIN CLEAR ACTION  ACNE MEDICATION TONER
    salicylic acid liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:62839-0138
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    Salicylic Acid (UNII: O414PZ4LPZ) (Salicylic Acid - UNII:O414PZ4LPZ) Salicylic Acid5 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    Water (UNII: 059QF0KO0R)  
    Butylene Glycol (UNII: 3XUS85K0RA)  
    Betaine (UNII: 3SCV180C9W)  
    Glycereth-26 (UNII: NNE56F2N14)  
    Methyl Gluceth-20 (UNII: J3QD0LD11P)  
    PPG-5-Ceteth-20 (UNII: 4AAN25P8P4)  
    Glycerin (UNII: PDC6A3C0OX)  
    Zinc Pidolate (UNII: C32PQ86DH4)  
    Phenoxyethanol (UNII: HIE492ZZ3T)  
    Chlorphenesin (UNII: I670DAL4SZ)  
    Phenylethyl Alcohol (UNII: ML9LGA7468)  
    Methylparaben (UNII: A2I8C7HI9T)  
    Benzoic Acid (UNII: 8SKN0B0MIM)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:62839-0138-7150 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product01/25/2002
    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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