DZUL ANTI-DANDRUFF

Manufacturer
Caball Sales, Inc.
Effective date
2026-01-08
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
monthly-update
Hydrated at
2026-06-03 17:52:37

Label at a glance#

ProductDZUL ANTI-DANDRUFF
Active ingredientPYRITHIONE ZINC
Label structure12 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Zinc Pyrithione 1%

OTC - PURPOSE SECTION

Anti-Dandruff

INDICATIONS & USAGE SECTION

For the relief of the symptoms of dandruff.

WARNINGS SECTION

For external use only.

Do not use on wounds or damaged skin or on a child under 12 years of age unless directed by a physician.

OTC - WHEN USING SECTION

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

OTC - STOP USE SECTION

Conditions worsens or does not improve after regular use of this product as directed.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

DOSAGE & ADMINISTRATION SECTION

Apply a small amount quantity of the product into hair and massage the scalp.
Rinse thoroughly with enough water, repeat if needed.

For best results, use at least twice a week or as directed by a doctor.

OTHER SAFETY INFORMATION

See on the bottom of the bottle for lot number and expiration date.

INACTIVE INGREDIENT SECTION

Water (Aqua), Sodium C14-16 Olefin Sulfonate, Cocamidopropyl Betaine, Acrylates Copolymer, Cocamide MEA, Cocamidopropylamine Oxide, Caprylyl Glycol, Hexylene Glycol, Fragrance (Parfum), Polyquaternium-7, Sodium Hydroxide, Disodium EDTA, Citric Acid, Panthenol, Phenoxyethanol, FD&C Blue No.1 (CI 42090), Hexyl Cinnamal, Benzyl Salicylate, Coumarin, Alpha-Isomethyl Ionone, Geraniol, Linalool.

OTC - QUESTIONS SECTION

QUESTION OR COMMENTS?

Call (305)-900-8256

DZUL ANTI-DANDRUFF SHAMPOO

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

DZUL ANTIDANDRUFF SHAMPOODZUL ANTIDANDRUFF SHAMPOO

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
209884zinc pyrithione 1 % Medicated ShampooPSN3
209884zinc pyrithione 10 MG/ML Medicated ShampooSCD3
209884zinc pyrithione 1 % Medicated ConditionerSY3
209884zinc pyrithione 1 % Medicated ShampooSY3

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
e2db08c6-133f-4f4f-afb4-e90a2418d6f6Product name120230320
3c386306-c48a-413e-bb69-70cb268496f3Product name120210727
ce6d5c06-3ae0-18a6-d5b3-8cd3cc0f8906Product name720210625
f52be47f-7aa7-46c0-b1fa-50c18dd50206Product name120201029
11ed6f83-cdd2-4637-8379-b1a1d3ae3cdeProduct name120181101
86c45a79-b9f0-4476-a27c-6e10db098497Product name120180125
d5e51f11-ad28-caa4-4b49-4143974782adProduct name120150831

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
83037-001-08DZUL ANTI-DANDRUFF236 mL in 1 BOTTLESHAMPOO2363

Products#

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

DailyMed product names page 1 of 1 · 23 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
83037-00183037-001-08

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 21 matching rows.

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
22024-11-22full-release2026-06-01 00:38:49

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
DZUL ANTI-DANDRUFFZINC PYRITHIONECaball Sales, Inc.05e3fac4-c0ce-cbb9-e063-6294a90ac0362026-01-08WarningsExact identifier
ndc (package): 83037-001-08
ndc (product): 83037-001
ndc11 (package): 83037000108
spl id: 47e60c2d-c9aa-e9c4-e063-6294a90afe19
spl set id: 05e3fac4-c0ce-cbb9-e063-6294a90ac036

Reported adverse events (FAERS/openFDA)#

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