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#
Contacts and useful links#
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
DailyMed RxNorm Mappings#
DailyMed Product Concepts#
| Product concept | Relation | Version | Effective |
|---|---|---|---|
| e2db08c6-133f-4f4f-afb4-e90a2418d6f6 | Product name | 1 | 20230320 |
| 3c386306-c48a-413e-bb69-70cb268496f3 | Product name | 1 | 20210727 |
| ce6d5c06-3ae0-18a6-d5b3-8cd3cc0f8906 | Product name | 7 | 20210625 |
| f52be47f-7aa7-46c0-b1fa-50c18dd50206 | Product name | 1 | 20201029 |
| 11ed6f83-cdd2-4637-8379-b1a1d3ae3cde | Product name | 1 | 20181101 |
| 86c45a79-b9f0-4476-a27c-6e10db098497 | Product name | 1 | 20180125 |
| d5e51f11-ad28-caa4-4b49-4143974782ad | Product name | 1 | 20150831 |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 83037-001-08 | DZUL ANTI-DANDRUFF | 236 mL in 1 BOTTLE | SHAMPOO | 236 | 3 |
Products#
Every source-derived product name is available through these pages.
- DZUL ANTI-DANDRUFF
- Zinc Pyrithione
- COCO MONOETHANOLAMIDE
- .ALPHA.-HEXYLCINNAMALDEHYDE
- ANHYDROUS CITRIC ACID
- SODIUM HYDROXIDE
- WATER
- PYRITHIONE ZINC
- SODIUM C14-16 OLEFIN SULFONATE
- COCAMIDOPROPYLAMINE OXIDE
- PHENOXYETHANOL
- FD&C BLUE NO. 1
- LINALOOL, (+)-
- BENZYL SALICYLATE
- COUMARIN
- PANTHENOL
- GERANIOL
- COCAMIDOPROPYL BETAINE
- CAPRYLYL GLYCOL
- EDETATE DISODIUM
- POLYQUATERNIUM-7 (70/30 ACRYLAMIDE/DADMAC; 1600 KD)
- ISOMETHYL-.ALPHA.-IONONE
- HEXYLENE GLYCOL
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 83037-001 | 83037-001-08 |
Ingredients#
Every source-derived ingredient row is available through these pages.
Source Document#
Older Hydrated Versions#
| Version | Effective date | Source | Hydrated |
|---|---|---|---|
| 2 | 2024-11-22 | full-release | 2026-06-01 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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| DZUL ANTI-DANDRUFF | ZINC PYRITHIONE | Caball Sales, Inc. | 05e3fac4-c0ce-cbb9-e063-6294a90ac036 | 2026-01-08 | Warnings | 83037-001-08 83037-001 83037000108 47e60c2d-c9aa-e9c4-e063-6294a90afe19 05e3fac4-c0ce-cbb9-e063-6294a90ac036 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
