Dermoia Dandruff Shampoo

Manufacturer
Treasurewise LLC | Pure Source, LLC
Effective date
2026-04-22
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:54:40

Label at a glance#

ProductDermoia Dandruff
Active ingredientPYRITHIONE ZINC
Label structure8 sections

Dosage and administration

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.

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Pyrithione Zinc 1.50 %

Purpose

OTC - PURPOSE SECTION

Anti-dandruff

Use(s)

INDICATIONS & USAGE SECTION

  • For relief of the symptoms of dandruff

Warnings:

WARNINGS SECTION

For external use only.

When using this product

OTC - WHEN USING SECTION

  • Avoid contact with the eyes
  • If contact occurs, rinse eyes thoroughly with water.

Stop use and ask a doctor if

OTC - STOP USE SECTION

  • condition worsens or does not improve after regular use of this product as directed

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

If pregnant or breast-feeding,

OTC - PREGNANCY OR BREAST FEEDING SECTION

ask a health professional before use

Directions:

DOSAGE & ADMINISTRATION SECTION

  • 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:

SPL UNCLASSIFIED SECTION

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

Inactive Ingredients:

INACTIVE INGREDIENT SECTION

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?

OTC - QUESTIONS SECTION

+1 786-321-8869

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label0Label0

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
426904zinc pyrithione 1.5 % Medicated ShampooPSN1
426904zinc pyrithione 15 MG/ML Medicated ShampooSCD1
426904zinc pyrithione 1.5 % Medicated ShampooSY1

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130199874551852GTIN-13: 0199874551852
EAN-13: 0199874551852
GTIN-12: 199874551852
UPC-A: 199874551852
GTIN storage (14 digits): 00199874551852
Label0.jpg

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
83524-965-00Dermoia Dandruff355 mL in 1 BOTTLESHAMPOO3551

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 32 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
83524-96583524-965-00

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 31 matching rows.

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Dermoia DandruffPYRITHIONE ZINCTreasurewise LLC7884bd3e-62ab-4fcd-8870-0a941c3feadb2026-04-22WarningsExact identifier
ndc (package): 83524-965-00
ndc (product): 83524-965
ndc11 (package): 83524096500
spl id: 50095406-028b-71a7-e063-6294a90ae3c2
spl set id: 7884bd3e-62ab-4fcd-8870-0a941c3feadb

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.