Label: DUOLAQ- salicylic acid gel
- NDC Code(s): 87110-001-01
- Packager: METHODIQ INC.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated November 10, 2025
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active ingredients
- Purpose
- Uses
- Warnings
-
Directions
- 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.
-
Inactive ingredients
Water, Glycerin, Ammonium Polyacryloyldimethyl Taurate, Propanediol, Sodium Polyacrylate, Butylene Glycol, Pentylene Glycol, Glycolic Acid, Dimethicone, Propylene Glycol, Dimethyl Isosorbide, 4-t-Butylcyclohexanol, Phenoxyethanol, Niacinamide, Xylitol, Caprylic Acid, Caprylyl Glycol, Allantoin, Hexylene Glycol, Ethylhexylglycerin, Chamomilla Recutita (Matricaria) Flower Extract, Hydrolyzed Sodium Hyaluronate, Citric Acid, Glycyrrhiza Glabra (Licorice) Root Powder, Fomes Officinalis (Mushroom) Extract, Camellia Oleifera Leaf Extract, Hydroxyphenyl Propamidobenzoic Acid, Leuconostoc/Radish Root Ferment Filtrate, Ascorbyl Palmitate, Potassium Sorbate, Sodium Benzoate, Triethyl Citrate, Phenethyl Alcohol, 2,6-Dimethyl-7-Octen-2-ol, Benzyl Acetate, Heliotropine, 3-Hexenol, Gamma-Undecalactone.
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
DUOLAQ
salicylic acid gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:87110-001 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID 20 mg in 1 mL Inactive Ingredients Ingredient Name Strength LARICIFOMES OFFICINALIS FRUITING BODY (UNII: 7IFM8431X3) PENTYLENE GLYCOL (UNII: 50C1307PZG) DIMETHYL ISOSORBIDE (UNII: SA6A6V432S) 4-T-BUTYLCYCLOHEXANOL (UNII: K0H1405S9C) TRIETHYL CITRATE (UNII: 8Z96QXD6UM) DIMETHICONE (UNII: 92RU3N3Y1O) ALLANTOIN (UNII: 344S277G0Z) NIACINAMIDE (UNII: 25X51I8RD4) GAMMA-UNDECALACTONE (UNII: QB1T0AG2YL) GLYCOLIC ACID (UNII: 0WT12SX38S) POTASSIUM SORBATE (UNII: 1VPU26JZZ4) CAPRYLIC ACID (UNII: OBL58JN025) CAPRYLYL GLYCOL (UNII: 00YIU5438U) CHAMOMILE (UNII: FGL3685T2X) SODIUM HYALURONATE (UNII: YSE9PPT4TH) CITRIC ACID (UNII: 2968PHW8QP) HYDROXYPHENYL PROPAMIDOBENZOIC ACID (UNII: 25KRT26H77) ASCORBYL PALMITATE (UNII: QN83US2B0N) HELIOTROPINE (UNII: KE109YAK00) WATER (UNII: 059QF0KO0R) GLYCERIN (UNII: PDC6A3C0OX) PHENETHYL ALCOHOL (UNII: ML9LGA7468) GLYCYRRHIZA GLABRA (LICORICE) ROOT POWDER (UNII: 2788Z9758H) CAMELLIA OLEIFERA LEAF (UNII: 5077EL0C60) SODIUM BENZOATE (UNII: OJ245FE5EU) PROPANEDIOL (UNII: 5965N8W85T) 2,6-DIMETHYL-7-OCTEN-2-OL (UNII: 46L1B02ND9) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) BENZYL ACETATE (UNII: 0ECG3V79ZJ) XYLITOL (UNII: VCQ006KQ1E) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) LEUCONOSTOC/RADISH ROOT FERMENT FILTRATE (UNII: D2QHA03458) 3-HEXENOL (UNII: V14F8G75P4) AMMONIUM POLYACRYLOYLDIMETHYL TAURATE (UNII: F01RIY4371) SODIUM POLYACRYLATE (8000 MW) (UNII: 285CYO341L) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) PHENOXYETHANOL (UNII: HIE492ZZ3T) HEXYLENE GLYCOL (UNII: KEH0A3F75J) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:87110-001-01 1 in 1 CARTON 11/18/2025 1 15 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M006 11/18/2025 Labeler - METHODIQ INC. (119377051)
