Label: CLEAR SMART BLEMISH SPOT TREATMENT- salicyclic acid gel

  • NDC Code(s): 68828-245-01
  • Packager: Jafra Cosmetics International Inc
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 28, 2023

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

  • ACTIVE INGREDIENT

    Active ingredient

    Salicylic Acid 1%

  • Purpose

    Acne treatment

  • Uses

    Treats acne
    Dries up acne pimples
    Helps prevent new acne pimples

  • Warnings

    For external use only

    When using this productusing other topical acne medications at the same time or immediately following the use of this product may increase dryness or irritation of the skin. If this occurs, only one medication should be used unless directed by a doctor.

  • 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.

  • Directions

    • Clean the skin thoroughly before applying
    • Cover the entire affected area with a thin layer 1 to 3 times daily
    • Avoid contact with eyes.
    • Because excessive drying may of the skin may occur, start with 1 application daily, then gradually increase to 2 or 3 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

    Allantoin, Bisabolol, Butylene Glycol, Butyrospermum Parkii (Shea) Butter, Carbomer, Decylene Glycol, Dipropylene Glycol, Disodium EDTA, Ethylhexylglycerin, Glycerin, Honey Extract, Hydrogenated Lecithin, Lecithin, Maltodextrin, Niacinamide, Phenethyl Alcohol, Phenoxyethanol, Spiraea Ulmaria Extract, Polyacrylate-13/Polyisobutene/ Polysorbate 20, Royal Jelly Powder, Royal Jelly, SD Alcohol 40-B, Sodium Hydroxide, Succinic Acid, Tetrapeptide-45, Water/Aqua, Zymomonas Ferment Extract.

  • Package label

    image description
  • INGREDIENTS AND APPEARANCE
    CLEAR SMART BLEMISH SPOT TREATMENT 
    salicyclic acid gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:68828-245
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID1 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    WATER (UNII: 059QF0KO0R)  
    SHEA BUTTER (UNII: K49155WL9Y)  
    ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    ALLANTOIN (UNII: 344S277G0Z)  
    NIACINAMIDE (UNII: 25X51I8RD4)  
    LEVOMENOL (UNII: 24WE03BX2T)  
    BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
    HONEY (UNII: Y9H1V576FH)  
    HYDROGENATED SOYBEAN LECITHIN (UNII: H1109Z9J4N)  
    MALTODEXTRIN (UNII: 7CVR7L4A2D)  
    LECITHIN, SOYBEAN (UNII: 1DI56QDM62)  
    PHENYLETHYL ALCOHOL (UNII: ML9LGA7468)  
    CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)  
    DECYLENE GLYCOL (UNII: S57M60MI88)  
    DIPROPYLENE GLYCOL (UNII: E107L85C40)  
    EDETATE DISODIUM (UNII: 7FLD91C86K)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    ROYAL JELLY (UNII: L497I37F0C)  
    ALCOHOL (UNII: 3K9958V90M)  
    SUCCINIC ACID (UNII: AB6MNQ6J6L)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:68828-245-0115 mL in 1 TUBE; Type 0: Not a Combination Product05/11/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00605/11/2020
    Labeler - Jafra Cosmetics International Inc (041676479)
    Establishment
    NameAddressID/FEIBusiness Operations
    Distribuidora Comercial Jafra, S.A. de C.V.951612777manufacture(68828-245)