Label: SERIOUS SKINCARE CONTINUOUSLY CLEAR ACNE MEDICATION FOR PROBLEMATIC SKIN DRY LO PRO ALL- OVER TREATMENT- salicylic acid lotion

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

Drug Label Information

Updated December 12, 2023

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

  • Drug Facts

  • Active ingredient

    Salicylic Acid 1%

    Purpose

    Acne Treatment

  • Uses

    • For the management of Acne
    • Reduce the number of Acne blemishes, blackheads, whiteheads, and allow skin to heal.
  • 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.

    Keep out of reach of children.

    If swallowed, get medical help or contact a Poison Control Center right away.

  • Directions

    • Shake before using. Apply the product on a cotton pad, then gently apply by tapping.
    • 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.
    • Avoid contact with eyes, eyelids and mucous membranes.
  • Inactive ingredients

    Aqua (Water), Alcohol Denat., Allantoin, Citrus Grandis (Grapefruit) Fruit Extract, Dipotassium Glycyrrhizate, Calendula Officinalis Flower Extract, Salix Alba (Willow) Bark Extract, Sulfur, Centella Asiatica Extract, Propylene Glycol, Sodium Citrate, Methylpropanediol, PEG-40 Hydrogenated Castor Oil, PEG-6 Caprylic/capric Glycerides, Polysorbate 20, Zinc Oxide, Magnesium Aluminum Silicate, Caprylyl Glycol, Phenylpropanol, Pyridoxine HCl, Maltodextrin, Silica, Citric Acid, Parfum (Fragrance), Phenoxyethanol, Sodium Benzoate, Potassium Sorbate, Iron Oxides (CI 77491).

  • Package Labeling:

    LabelBox

  • INGREDIENTS AND APPEARANCE
    SERIOUS SKINCARE CONTINUOUSLY CLEAR ACNE MEDICATION FOR PROBLEMATIC SKIN DRY LO PRO ALL- OVER TREATMENT 
    salicylic acid lotion
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:53755-110
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID10 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    ALCOHOL (UNII: 3K9958V90M)  
    ALLANTOIN (UNII: 344S277G0Z)  
    PUMMELO (UNII: ET1TN5W71X)  
    GLYCYRRHIZINATE DIPOTASSIUM (UNII: CA2Y0FE3FX)  
    CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD)  
    SALIX ALBA BARK (UNII: 205MXS71H7)  
    SULFUR (UNII: 70FD1KFU70)  
    CENTELLA ASIATICA (UNII: 7M867G6T1U)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    SODIUM CITRATE (UNII: 1Q73Q2JULR)  
    METHYLPROPANEDIOL (UNII: N8F53B3R4R)  
    POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F)  
    PEG-6 CAPRYLIC/CAPRIC GLYCERIDES (UNII: GO50W2HWO8)  
    POLYSORBATE 20 (UNII: 7T1F30V5YH)  
    ZINC OXIDE (UNII: SOI2LOH54Z)  
    MAGNESIUM ALUMINUM SILICATE (UNII: 6M3P64V0NC)  
    CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
    PHENYLPROPANOL (UNII: 0F897O3O4M)  
    PYRIDOXINE HYDROCHLORIDE (UNII: 68Y4CF58BV)  
    MALTODEXTRIN (UNII: 7CVR7L4A2D)  
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    SODIUM BENZOATE (UNII: OJ245FE5EU)  
    POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
    FERRIC OXIDE RED (UNII: 1K09F3G675)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:53755-110-001 in 1 BOX06/01/2018
    1200 mL in 1 BOTTLE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00606/01/2018
    Labeler - Flageoli Limited (036999498)