Label: KADASON MEDICATED- salicylic acid shampoo
- NDC Code(s): 87263-927-00
- Packager: Ys Pharma Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 10, 2025
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- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Drug Facts
- Active Ingredients
- Uses
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Warnings:
For external use only
When using this product
- Avoid contact with the eyes.
- If contact occurs, rinse eyes thoroughly with water.
Stop use and ask a doctor if
condition worsens or does not improve after regular use of this product as directed
- Directions:
- Other information:
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Inactive ingredients
Water (Aqua), Sodium Lauryl Methyl Isethionate, Sodium C14-16 Olefin Sulfonate, Sodium Lauroamphoacetate, Alcohol, Cocamidopropyl Betaine, Sodium Cocoyl Isethionate, Propanediol, Butylene Glycol, Camellia Sinensis Leaf Extract, Guar Hydroxypropyltrimonium Chloride, Glycerin, Aloe Barbadensis Leaf Juice, Hydroxyethylcellulose, Aminomethyl Propanol, Tremella Fuciformis (Mushroom) Extract, Polyquaternium-10, Ganoderma Lucidum (Mushroom) Extract, Cocamide MEA, Dipotassium Glycyrrhizate, Bacillus/Glycine Soja (Soybean) Ferment Extract, PEG-120 Methyl Glucose Dioleate, Phenoxyethanol, Ethylhexylglycerin
- Questions?
- Package Labeling:
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INGREDIENTS AND APPEARANCE
KADASON MEDICATED
salicylic acid shampooProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:87263-927 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID 18 mg in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) SODIUM LAUROYL METHYL ISETHIONATE (UNII: II6VCD3S6R) SODIUM C14-16 OLEFIN SULFONATE (UNII: O9W3D3YF5U) SODIUM LAUROAMPHOACETATE (UNII: SLK428451L) ALCOHOL (UNII: 3K9958V90M) COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX) SODIUM COCOYL ISETHIONATE (UNII: 518XTE8493) PROPANEDIOL (UNII: 5965N8W85T) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) GREEN TEA LEAF (UNII: W2ZU1RY8B0) GUAR HYDROXYPROPYLTRIMONIUM CHLORIDE (UNII: B16G315W7A) GLYCERIN (UNII: PDC6A3C0OX) ALOE VERA LEAF JUICE (UNII: RUE8E6T4NB) HYDROXYETHYLCELLULOSE (UNII: T4V6TWG28D) AMINOMETHYL PROPANOL (UNII: LU49E6626Q) TREMELLA FUCIFORMIS FRUITING BODY (UNII: GG8N28393G) REISHI (UNII: TKD8LH0X2Z) COCO MONOETHANOLAMIDE (UNII: C80684146D) DIPOTASSIUM GLYCYRRHIZATE (UNII: CA2Y0FE3FX) SOYBEAN (UNII: L7HT8F1ZOD) PEG-120 METHYL GLUCOSE DIOLEATE (UNII: YM0K64F20V) PHENOXYETHANOL (UNII: HIE492ZZ3T) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:87263-927-00 237 mL in 1 BOTTLE; Type 0: Not a Combination Product 11/06/2025 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M032 11/06/2025 Labeler - Ys Pharma Inc. (137354172) Registrant - Pure Source, LLC (080354456)

