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Dermalogica Oil Control (PureTek Corporation)

Available Formats

Dosage Form Package Information Links
LOTION 1 TUBE in 1 CARTON (59088-737-05) > 60 mL in 1 TUBE Label Information

Complete Dermalogica Oil Control Information

  • Active ingredient

    Salicylic Acid (1.0%)


  • Purpose

    Acne Treatment


  • Keep out of reach of children.

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



  • Use

    Treats acne


  • Warnings

    For external use only.
  • Directions

    • Apply to cleansed face and throat twice daily.
    • Avoid eye area.



  • Inactive ingredients

    Water (Aqua), Butylene Glycol, C12-15 Alkyl Benzoate, Isododecane, Potato Starch Modified, Silica, Hyssopus Officinalis Extract, Melissa Officinalis Leaf Extract, Echinacea Purpurea Extract, Enantia Chlorantha Bark Extract, Yeast Extract, Aesculus Hippocastanum (Horse Chestnut) Seed Extract, Salix Nigra (Willow) Bark Extract, Allantoin, Panthenol, Sodium PCA, Bisabolol, Niacinamide, Ammonium Glycyrrhizate, Zinc Gluconate, Caffeine, Biotin, Phospholipids, Magnesium Ascorbyl Phosphate, Camphor, Menthol, Hamamelis Virginiana (Witch Hazel) Water, Oleanolic Acid, Sodium Hydroxide, Potassium Cetyl Phosphate, Glyceryl Stearate, PEG-100 Stearate, Cetyl Alcohol, Xanthan Gum, Vinyl Dimethicone/Methicone Silsesquioxane Crosspolymer, Nylon-12, Glycerin, Disodium EDTA, Ethylhexylglycerin, Phenoxyethanol.


  • Do not use

    • Do not use around eye area
    • If contact occurs, flush thoroughly with water.
    • if irritation develops, discontinue use

  • When using this product

    If dryness or irritation occurs when using other topical acne products at the same time, limit usage to one acne product.
  • INGREDIENTS AND APPEARANCE
    DERMALOGICA OIL CONTROL 
    salicylic acid lotion
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:59088-737
    Route of Administration TOPICAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID 10 uL  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    WATER (UNII: 059QF0KO0R)  
    BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
    ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)  
    ISODODECANE (UNII: A8289P68Y2)  
    STARCH, POTATO (UNII: 8I089SAH3T)  
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
    MELISSA OFFICINALIS (UNII: YF70189L0N)  
    ECHINACEA PURPUREA (UNII: QI7G114Y98)  
    YEAST (UNII: 3NY3SM6B8U)  
    HORSE CHESTNUT (UNII: 3C18L6RJAZ)  
    SALIX NIGRA BARK (UNII: QU52J3A5B3)  
    ALLANTOIN (UNII: 344S277G0Z)  
    PANTHENOL (UNII: WV9CM0O67Z)  
    SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2)  
    LEVOMENOL (UNII: 24WE03BX2T)  
    NIACINAMIDE (UNII: 25X51I8RD4)  
    GLYCYRRHIZIN, AMMONIATED (UNII: 3VRD35U26C)  
    ZINC GLUCONATE (UNII: U6WSN5SQ1Z)  
    CAFFEINE (UNII: 3G6A5W338E)  
    BIOTIN (UNII: 6SO6U10H04)  
    LECITHIN, SOYBEAN (UNII: 1DI56QDM62)  
    MAGNESIUM ASCORBYL PHOSPHATE (UNII: 0R822556M5)  
    CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET)  
    MENTHOL (UNII: L7T10EIP3A)  
    OLEANOLIC ACID (UNII: 6SMK8R7TGJ)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    POTASSIUM CETYL PHOSPHATE (UNII: 03KCY6P7UT)  
    GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  
    POLYOXYL 100 STEARATE (UNII: YD01N1999R)  
    CETYL ALCOHOL (UNII: 936JST6JCN)  
    XANTHAN GUM (UNII: TTV12P4NEE)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    EDETATE DISODIUM (UNII: 7FLD91C86K)  
    ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    HAMAMELIS VIRGINIANA LEAF WATER (UNII: 8FP93ED6H2)  
    HYSSOP (UNII: X7HKN4FOJI)  
    ANNICKIA CHLORANTHA BARK (UNII: H70115MP4A)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:59088-737-05 1 in 1 CARTON
    1 60 mL in 1 TUBE
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC monograph final part333D 11/17/2003
    Labeler - PureTek Corporation (785961046)
    Establishment
    Name Address ID/FEI Business Operations
    PureTek Corporation 785961046 manufacture, label, pack, outsourcing human drug compounding, relabel, repack
    Establishment
    Name Address ID/FEI Business Operations
    PureTek Corporation 031678746 manufacture, label, pack, outsourcing human drug compounding, relabel, repack