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
- 66f301bf-8e2e-43ce-b6b8-0983fe795f01
- SPL ID
- 4af72577-4c37-3fb0-e063-6394a90a214b
- Version
- 17
- Effective date
- 2026-02-16
- Source export date
- 2026-10-12
- Source partition
- 13
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0013-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-12/b8dac220ac9fc8ffb4d86c6e00ece30169fc4575ca0cc92e5c9ce1a524fb0249/drug-label-0013-of-0014.json.zip
- Source manifest SHA-256
- 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
- Import run
- 20261013T011858Z
- Imported at
- 2026-10-13 03:11:45
| 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 | 41163-153-32 | openfda.package_ndc |
| ndc | package | 41163-153-15 | openfda.package_ndc |
| ndc | package | 41163-153-40 | openfda.package_ndc |
| ndc | package | 41163-153-35 | openfda.package_ndc |
| ndc | product | 41163-153 | openfda.product_ndc |
| ndc11 | package | 41163015335 | derived:openfda.package_ndc |
| ndc11 | package | 41163015340 | derived:openfda.package_ndc |
| ndc11 | package | 41163015315 | derived:openfda.package_ndc |
| ndc11 | package | 41163015332 | derived:openfda.package_ndc |
| rxcui | 209884 | openfda.rxcui | |
| spl id | 4af72577-4c37-3fb0-e063-6394a90a214b | id | |
| spl set id | 66f301bf-8e2e-43ce-b6b8-0983fe795f01 | 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.