Label: NATURIUM SALICYLIC ACID SERUM 2%- salicylic acid liquid

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated November 14, 2023

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  • Drug Facts

  • Active Ingredient

    Salicylic Acid 2.00%

  • Purpose

    Acne Treatment

  • Uses

    • Helps fight existing acne breakouts and prevents future acne breakouts.
  • Warnings

    For external use only.

    When using this product

    • skin irritation and dryness are more likely to occur when using another topical acne product at the same time. If irritation occurs, use only one acne product at a time.
    • Avoid eye area. In case of eye contact, flush gently and thoroughly with water. Do not apply to broken or irritated skin.

    Keep out of reach of children.

    If swallowed, seek medical help.

  • Directions

    Shake Well.

    • clean the skin thoroughly before applying this product.
    • cover the entire affected area with a thin layer one to three times daily.
    • because excessive drying of the skin may occur, start with one application daily, then gradually increase to two or three times daily if needed or as directed by a doctor.
    • if bothersome dryness or peeling occurs, reduce application to once a day or every other day.
    • if going outside, apply sunscreen after using this product. If irritation or sensitivity develops, stop use and ask a doctor.
  • Other Information

    Sensitivity Test for a New User. Apply product sparingly to one or two small affected areas during the first 3 days. If no discomfort occurs, follow the directions stated above. Store in controlled temperatures (4-20°C/39-68°F). Keep in a dark and dry place. Keep container tightly closed.

  • Inactive Ingredients

    Aqua (Water), Propanediol, Sodium Polyacrylate, Maltobionic Acid, Amorphophallus Konjac Root Extract, Caprylyl Glycol, Phenoxyethanol, Carbomer, Dipropylene Glycol, Sodium Phytate, Sodium Hydroxide, Xanthan Gum.

  • Product Packaging

    1

  • INGREDIENTS AND APPEARANCE
    NATURIUM SALICYLIC ACID SERUM 2% 
    salicylic acid liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:76354-122
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID20 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    MALTOBIONIC ACID (UNII: 47RDD4XT2O)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    XANTHAN GUM (UNII: TTV12P4NEE)  
    DIPROPYLENE GLYCOL (UNII: E107L85C40)  
    WATER (UNII: 059QF0KO0R)  
    SODIUM POLYACRYLATE (8000 MW) (UNII: 285CYO341L)  
    PROPANEDIOL (UNII: 5965N8W85T)  
    AMORPHOPHALLUS KONJAC ROOT (UNII: F7KU2UY3HE)  
    CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
    PHYTATE SODIUM (UNII: 88496G1ERL)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:76354-122-011 in 1 CARTON06/17/2022
    130 mL in 1 BOTTLE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00606/17/2022
    Labeler - e.l.f. Cosmetics, Inc (093902816)
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