warnings
Warnings For external use only
Dandruff
openFDA label record#
This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.
Verified complete openFDA source JSON
- Brand name
- Dandruff
- Generic name
- PYRITHIONE ZINC
- Manufacturer
- United Natural Foods, Inc. dba UNFI
- Product type
- HUMAN OTC DRUG
- SPL set ID
- d7c4507e-7f74-4bcd-9b0e-0b097193a1a8
- SPL ID
- 4b06c184-4d5b-4838-e063-6294a90a8176
- Version
- 16
- Effective date
- 2026-02-17
- Source export date
- 2026-09-28
- Source partition
- 4
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0004-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/c7ca0b7091cdaeab3f27713a6eef00adcf8fe722383633ddce61531b4c840544/drug-label-0004-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 05:25:57
| Harmonized routes |
|---|
| TOPICAL |
Harmonized identifier links#
Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.
| Type | Scope | Identifier | Source field |
|---|---|---|---|
| application number | M032 | openfda.application_number | |
| brand name | Dandruff | openfda.brand_name | |
| generic name | PYRITHIONE ZINC | openfda.generic_name | |
| manufacturer name | United Natural Foods, Inc. dba UNFI | openfda.manufacturer_name | |
| ndc | package | 41163-024-35 | openfda.package_ndc |
| ndc | package | 41163-024-40 | openfda.package_ndc |
| ndc | package | 41163-024-15 | openfda.package_ndc |
| ndc | package | 41163-024-32 | openfda.package_ndc |
| ndc | product | 41163-024 | openfda.product_ndc |
| ndc11 | package | 41163002435 | derived:openfda.package_ndc |
| ndc11 | package | 41163002440 | derived:openfda.package_ndc |
| ndc11 | package | 41163002432 | derived:openfda.package_ndc |
| ndc11 | package | 41163002415 | derived:openfda.package_ndc |
| rxcui | 209884 | openfda.rxcui | |
| spl id | 4b06c184-4d5b-4838-e063-6294a90a8176 | id | |
| spl set id | d7c4507e-7f74-4bcd-9b0e-0b097193a1a8 | set_id | |
| unii | R953O2RHZ5 | openfda.unii |
Warnings cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
Adverse reactions cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
adverse reactions
Adverse Reactions Like it or let us make it right. That's our quality promise. 855-423-2630 DISTRIBUTED BY UNFI PROVIDENCE, RI 02908 USA
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.