Label: PERRICONE ACNE RELIEF GENTLE EXFOLIATING TONER- salicylic acid solution

  • 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 September 11, 2021

If you are a consumer or patient please visit this version.

  • Drug Facts

    Active Ingredient

    Salicylic Acid (2.0%)

  • PURPOSE

    Purpose
    Acne Treatment

  • INDICATIONS & USAGE

    Use ■ For the treatment of acne.

  • WARNINGS

    Warnings
    For external use only.

    Keep out of eyes. If product enters the eyes,
    wash out thoroughly with warm water.

    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

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

  • DOSAGE & ADMINISTRATION

    Directions
    ■ clean the skin thoroughly before applying
       this product.
    ■ cover the entire affected area with a thin
       layer morning & evening. No rinsing is
       needed. Wait until dry before applying
       treatment or moisturizer.
    ■ 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 INGREDIENT

    Inactive ingredients Water/Aqua/Eau, SD
    Alcohol 40-B, Dimethyl MEA, Phenoxyethanol,
    PPG-26-Buteth-26, PEG-40 Hydrogenated
    Castor Oil, Disodium EDTA, Glycerin, Magnesium
    Aspartate, Zinc Gluconate, Lactic Acid, Acetyl
    Tyrosine, Succinic Acid, Citrulline, Butylene
    Glycol, Copper Gluconate, Sodium Hyaluronate,
    Tetrapeptide-21

  • QUESTIONS

    Questions?1-888-823-7837

  • Product Label

    Perricone MD

    ACNE RELIEF

    Gentle
    Exfoliating
    Toner

    Salicylic Acid Acne Treatment

    Lactic & Succinic Acids, Salicylic Acid,
    Citrulline

    ℮ 118 mL / 4 US fl. oz.

    Dist. By: NV Perricone LLC. Shepherdsville, KY
    40165. Made in USA of foreign and domestic
    components. Perricone MD, a THG brand THG
    Beauty Limited Voyager House, M90 3DQ, UK
    73 Rue Saint-Anne, 75002, Paris, FR. 651362

    1 888 823 7837
    perriconemd.com

    157 Exfoliating

    157 Exfoliating Jar

    res

  • INGREDIENTS AND APPEARANCE
    PERRICONE ACNE RELIEF GENTLE EXFOLIATING TONER 
    salicylic acid solution
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:54111-157
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID2.0 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    ALCOHOL (UNII: 3K9958V90M)  
    DEANOL (UNII: 2N6K9DRA24)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    PPG-26-BUTETH-26 (UNII: 2II1K6TZ4P)  
    POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F)  
    EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    MAGNESIUM ASPARTATE (UNII: R17X820ROL)  
    ZINC GLUCONATE (UNII: U6WSN5SQ1Z)  
    LACTIC ACID (UNII: 33X04XA5AT)  
    ACETYL L-TYROSINE (UNII: DA8G610ZO5)  
    SUCCINIC ACID (UNII: AB6MNQ6J6L)  
    CITRULLINE (UNII: 29VT07BGDA)  
    BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
    COPPER GLUCONATE (UNII: RV823G6G67)  
    HYALURONATE SODIUM (UNII: YSE9PPT4TH)  
    TETRAPEPTIDE-21 (UNII: 179JUC43HU)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:54111-157-501 in 1 CARTON12/01/2021
    1118 mL in 1 BOTTLE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart333D12/01/2021
    Labeler - Bentley Laboratories, LLC (068351753)
    Registrant - Bentley Laboratories, LLC (068351753)