KADASON MEDICATED- salicylic acid shampoo

Kadason Medicated by

Drug Labeling and Warnings

Kadason Medicated by is a Otc medication manufactured, distributed, or labeled by Ys Pharma Inc., Pure Source, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active Ingredients

Salicylic Acid 1.80 %

Purpose

Seborrheic Dermatitis

Uses

• For relief of the symptoms of seborrheic dermatitis.

Warnings:

For external use only

Do not use

for prolonged periods without consulting a doctor

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

Keep out of reach of children.

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

If pregnant or breast-feeding,

ask a health professional before use

Directions:

• wet hair
• apply shampoo and work into a lather
• rinse thoroughly 
• for best results, use at least twice a week or as directed by a doctor

Other information:

• Protect the product in this container from excessive heat and direct sun.

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?

1-800-256-7159

Package Labeling:

INGREDIENTS AND APPEARANCE

KADASON MEDICATED 
salicylic acid shampoo

Product 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)