Label: PERFECT ME SERUM- salicylic acid cream

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved drug other

Drug Label Information

Updated 02/13

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  • ACTIVE INGREDIENT

    ACTIVE INGREDIENTS
    Salicyclic Acid (0.5%)
    KEY INGREDIENTS
    Azelaic Acid and Oleanolic Acid Close
  • PURPOSE

    PERFECT-ME SERUM
    with Salicyclic Acid
    Acne Treatment Close
  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children.

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  • INDICATIONS & USAGE

    PERFECT-ME SERUM LANGE
    INDICATIONS: For the Management of Acne
    This non-oily and lightely scented treatment serum has been specially formulated for acne-prone skin. With a light, fresh texture, this pleasant will contribute to:
    Help clear blackheads,
    Help prevent the development of new acne pimples,
    Allow skin to heal.

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  • WARNINGS

    Not to be used for children under three years of age. Avoid contact with Eyes.
    For external use only. If skin has allergic reaction, stop use immediately.

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  • DOSAGE & ADMINISTRATION

    20 ml
    0.68 FL. OZ Close
  • INACTIVE INGREDIENT

    WATER
    PROPYLENE GLYCOL
    POLYMETHYL METHACRYLATE
    POTASSIUM AZELOYL DIGLYCINATE
    GLYCERIN
    CARBOMER
    OLEANOLIC ACID
    HYDROXYETHYL ACRYLATE/SODIUM
    ACRYLOYLDIMETHYLTAURATE
    COPOLYMER
    SQUALANE
    CHITOSAN SUCCINAMIDE
    XANTHAN GUM
    SALICYLIC ACID
    BUTYLENE GLYCOL
    PEG-60 ALMOND GLYCERIDES
    CAPRYLYL GLYCOL
    POLYSORBATE 60
    SODIUM LACTATE
    DISODIUM SUCCINATE
    SODIUM CITRATE
    CITRIC ACID
    BIOTIN
    BENZYL BENZOATE
    HEXYL CINNAMAL
    CITRONELLOL
    ALPHA-ISOMETHYL IONONE
    GERANIOL
    EUGENOL
    LIMONENE
    LINALOOL
    NORDIHYDROGUAIARETIC ACID
    SODIUM METABISULFITE
    CHLORPHENESIN
    PHENOXYETHANOL
    METHYLPARABEN
    SODIUM METHYLPARABEN
    BUTYLPARABEN
    ETHYLPARABEN
    PROPYLPARABEN
    ISOBUTYLPARABEN
    CI 77891 (TITANIUM DIOXIDE) Close
  • INGREDIENTS AND APPEARANCE
    PERFECT ME SERUM 
    salicylic acid cream
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:51830-052
    Route of Administration TOPICAL DEA Schedule     
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID 1 mg  in 20 mg
    Inactive Ingredients
    Ingredient Name Strength
    WATER (UNII: 059QF0KO0R)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    POTASSIUM AZELOYL DIGLYCINATE (UNII: N02RVN6NYP)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    OLEANOLIC ACID (UNII: 6SMK8R7TGJ)  
    HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER (45000 MPA.S AT 1%) (UNII: 86FQE96TZ4)  
    SQUALANE (UNII: GW89575KF9)  
    XANTHAN GUM (UNII: TTV12P4NEE)  
    BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
    PEG-60 ALMOND GLYCERIDES (UNII: 4Y0E651N0F)  
    CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
    POLYSORBATE 60 (UNII: CAL22UVI4M)  
    SODIUM LACTATE (UNII: TU7HW0W0QT)  
    SODIUM SUCCINATE ANHYDROUS (UNII: V8ZGC8ISR3)  
    SODIUM CITRATE (UNII: 1Q73Q2JULR)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    BIOTIN (UNII: 6SO6U10H04)  
    BENZYL BENZOATE (UNII: N863NB338G)  
    .ALPHA.-HEXYLCINNAMALDEHYDE (UNII: 7X6O37OK2I)  
    .BETA.-CITRONELLOL, (R)- (UNII: P01OUT964K)  
    ISOMETHYL-.ALPHA.-IONONE (UNII: 9XP4LC555B)  
    GERANIOL (UNII: L837108USY)  
    EUGENOL (UNII: 3T8H1794QW)  
    LINALOOL, (+)- (UNII: F4VNO44C09)  
    MASOPROCOL (UNII: 7BO8G1BYQU)  
    SODIUM METABISULFITE (UNII: 4VON5FNS3C)  
    CHLORPHENESIN (UNII: I670DAL4SZ)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    METHYLPARABEN (UNII: A2I8C7HI9T)  
    METHYLPARABEN SODIUM (UNII: CR6K9C2NHK)  
    BUTYLPARABEN (UNII: 3QPI1U3FV8)  
    ETHYLPARABEN (UNII: 14255EXE39)  
    PROPYLPARABEN (UNII: Z8IX2SC1OH)  
    ISOBUTYLPARABEN (UNII: 0QQJ25X58G)  
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:51830-052-08 20 mg in 1 BOX
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    unapproved drug other 07/18/2012
    Labeler - Lange SAS (275956105)
    Establishment
    Name Address ID/FEI Business Operations
    Lange SAS 275956105 manufacture(51830-052)
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