DERMOIA DANDRUFF- pyrithione zinc shampoo

Drug Labeling and Warnings

Drug Details [pdf]

Drug Facts

Active Ingredients

Pyrithione Zinc 1.50 %

Purpose

Anti-dandruff

Use(s)

• For relief of the symptoms of dandruff

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

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:

• Apply and then wash off after brief (a few minutes) exposure.
• 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:

Aloe Barbadensis Leaf Juice, Argania Spinosa Kernel Oil, Biotin, Camellia Sinensis (Green Tea) Leaf Extract, Caprylhydroxamic Acid, Ceramide NG, Cocamidopropyl Betaine, Collagen, Dicalcium Phosphate, Glycerin, Glyceryl Caprylate, Hydrolyzed Keratin, Lactobacillus Ferment, Laminaria Digitata Extract, Lauryl Glucoside, Leuconostoc/Radish Root Ferment Filtrate, Melaleuca Alternifolia (Tea Tree) Leaf Oil, Mentha Piperita (Peppermint) Oil, Menthol, Niacinamide, Panthenol, PEG-60 Hydrogenated Castor Oil, PEG-8, Polyacrylate-1 Crosspolymer, Salicylic Acid, Sodium Benzoate, Sodium C14-16 Olefin Sulfonate, Sodium Chloride, Sodium Cocoyl Isethionate, Sodium Hydroxide, Sodium Lauryl Glucose Carboxylate, Squalane, Tuber Aestivum Extract, Water (Aqua)

Questions?

+1 786-321-8869

Package Labeling:

INGREDIENTS AND APPEARANCE

DERMOIA DANDRUFF 
pyrithione zinc shampoo

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 83524-965
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
PYRITHIONE ZINC (UNII: R953O2RHZ5) (PYRITHIONE ZINC - UNII:R953O2RHZ5)	PYRITHIONE ZINC	15 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
ALOE BARBADENSIS LEAF JUICE (UNII: RUE8E6T4NB)
ARGAN OIL (UNII: 4V59G5UW9X)
BIOTIN (UNII: 6SO6U10H04)
GREEN TEA LEAF (UNII: W2ZU1RY8B0)
CAPRYLHYDROXAMIC ACID (UNII: UPY805K99W)
CERAMIDE NG (UNII: C04977SRJ5)
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
ANHYDROUS DIBASIC CALCIUM PHOSPHATE (UNII: L11K75P92J)
GLYCERIN (UNII: PDC6A3C0OX)
GLYCERYL MONOCAPRYLATE (UNII: TM2TZD4G4A)
LAMINARIA DIGITATA (UNII: 15E7C67EE8)
LAURYL GLUCOSIDE (UNII: 76LN7P7UCU)
LEUCONOSTOC/RADISH ROOT FERMENT FILTRATE (UNII: D2QHA03458)
TEA TREE OIL (UNII: VIF565UC2G)
PEPPERMINT OIL (UNII: AV092KU4JH)
MENTHOL (UNII: L7T10EIP3A)
NIACINAMIDE (UNII: 25X51I8RD4)
PANTHENOL (UNII: WV9CM0O67Z)
PEG-60 HYDROGENATED CASTOR OIL (UNII: 02NG325BQG)
POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)
POLYACRYLATE-1 CROSSPOLYMER (UNII: R5P9Z5WD6D)
SALICYLIC ACID (UNII: O414PZ4LPZ)
SODIUM BENZOATE (UNII: OJ245FE5EU)
SODIUM C14-16 OLEFIN SULFONATE (UNII: O9W3D3YF5U)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
SODIUM COCOYL ISETHIONATE (UNII: 518XTE8493)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
SQUALANE (UNII: GW89575KF9)
SUMMER TRUFFLE (UNII: Q95E62WF78)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 83524-965-00	355 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/14/2026

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M032	04/14/2026

Labeler - Treasurewise LLC (112606067)

Registrant - Pure Source, LLC (080354456)