Label: CLARIFYING TONER- salicylic acid liquid

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

Drug Label Information

Updated April 9, 2025

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  • Drug Facts

  • ​Active ingredient

    Salicylic Acid 2%

  • ​Purpose

    Acne Treatment

  • ​Use

    For the treatment of acne

  • ​Warnings

    For external use only.

    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. • Avoid contact with eyes, lips and mouth. If contact occurs, flush thoroughly with water.

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

  • ​Directions

    • Spray toner directly on face or on cotton pad. Apply to face and neck, avoiding the eye area. Repeat until minimal dirt is visible. Can be used twice daily or as directed by a physician.

  • ​Inactive ingredients

    Water, PPG-26-Buteth-26, PEG-40 Hydrogenated Castor Oil, Glycerin, Carica Papaya (Papaya) Fruit Extract, Olea Europaea (Olive) Leaf Extract, Rosmarinus Officinalis (Rosemary) Leaf Extract, Beta-Glucan, Allantoin, Panthenol, Sodium PCA, Menthyl Lactate, Benzophenone-4, Sodium Hydroxide, Methylchloroisothiazolinone, Methylisothiazolinone, Fragrance (Parfum), Blue 1

  • SPL UNCLASSIFIED SECTION

    ​MEDICAL GRADE SKIN CARE

    REPAIR

    cleanse//exfoliate

    Made in USA

    Dist. by DRMTLGY, LLC
    Chatsworth, CA 91311
    www.DRMTLGY.com

  • Packaging

    CLARIFYING TONER

  • INGREDIENTS AND APPEARANCE
    CLARIFYING TONER 
    salicylic acid liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:83286-012
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID2 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    PPG-26-BUTETH-26 (UNII: 2II1K6TZ4P)  
    POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    PAPAYA (UNII: KU94FIY6JB)  
    OLEA EUROPAEA (OLIVE) LEAF POWDER (UNII: MJ95C3OH47)  
    ROSEMARY (UNII: IJ67X351P9)  
    YEAST .BETA.-D-GLUCAN (UNII: 44FQ49X6UN)  
    ALLANTOIN (UNII: 344S277G0Z)  
    PANTHENOL (UNII: WV9CM0O67Z)  
    SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2)  
    MENTHYL LACTATE, (-)- (UNII: 2BF9E65L7I)  
    SULISOBENZONE (UNII: 1W6L629B4K)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)  
    METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)  
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:83286-012-01189 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product04/08/2025
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00604/08/2025
    Labeler - Drmtlgy, LLC (094762235)
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