Label: NATURIUM SALICYLIC ACID BODY 2%- salicylic acid aerosol, spray

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

Drug Label Information

Updated November 15, 2023

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  • Drug Facts

  • Active Ingredient

    Salicylic Acid 2.0%

  • Purpose

    Acne Treatment

  • Uses

    • For the treatment of acne.
    • Clears acne blemishes and allows skin to heal.
    • Helps prevent new acne blemishes from forming.
  • Warnings

    For external use only.

    Contents under pressure. Do not puncture or incinerate. Do not store at temperatures above 120F.

    When using this product

    • Skin irritation and dryness is more likely to occur if you use another topical acne medication at the same time. If irritation occurs, only use one topical acne medication at a time.

    Keep out of reach of children.

  • 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.
  • Inactive Ingredients

    WATER, NIACINAMIDE, ACETYL GLUCOSAMINE, HYDROLYZED OAT PROTEIN, GALACTOMYCES FERMENT FILTRATE, HYDROLYZED CICER SEED EXTRACT, MEDICAGO SATIVA (ALFALFA) EXTRACT, PUERARIA LOBATA ROOT EXTRACT, SILYBUM MARIANUM SEED EXTRACT, AMYLOPECTIN, DEXTRIN, 3-O-ETHYL ASCORBIC ACID, ALPHA-ARBUTIN, POLYDEXTROSE, HYDROXYACETOPHENONE, SODIUM GLUCONATE, POTASSIUM SORBATE, SODIUM BENZOATE, BUTYLENE GLYCOL

  • Questions?

    Visit www.naturium.com

  • Product Packaging

    1

  • INGREDIENTS AND APPEARANCE
    NATURIUM SALICYLIC ACID BODY 2% 
    salicylic acid aerosol, spray
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:76354-124
    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
    PUERARIA MONTANA VAR. LOBATA ROOT (UNII: PET93F4I3C)  
    AMYLOPECTIN, UNSPECIFIED SOURCE (UNII: 4XO4QFV777)  
    MEDICAGO SATIVA WHOLE (UNII: DJO934BRBD)  
    SILYBUM MARIANUM SEED (UNII: U946SH95EE)  
    3-O-ETHYL ASCORBIC ACID (UNII: 6MW60CB71P)  
    ICODEXTRIN (UNII: 2NX48Z0A9G)  
    SODIUM GLUCONATE (UNII: R6Q3791S76)  
    POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
    SODIUM BENZOATE (UNII: OJ245FE5EU)  
    N-ACETYLGLUCOSAMINE (UNII: V956696549)  
    HYDROXYACETOPHENONE (UNII: G1L3HT4CMH)  
    NIACINAMIDE (UNII: 25X51I8RD4)  
    BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
    WATER (UNII: 059QF0KO0R)  
    ALPHA-ARBUTIN (UNII: 72VUP07IT5)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:76354-124-01120 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product12/01/2022
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00612/01/2022
    Labeler - e.l.f. Cosmetics, Inc (093902816)
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