warnings
Warnings For external use only
Redken 5th Avenue NYC Scalp Relief Dandruff Control
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
- Redken 5th Avenue NYC Scalp Relief Dandruff Control
- Generic name
- PYRITHIONE ZINC
- Manufacturer
- L'Oreal USA Products Inc
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 306a1ef4-e7ed-4c8c-877c-3c34d3e6d7b7
- SPL ID
- 099d44dc-eff9-47d9-b252-e9f633f0016b
- Version
- 9
- Effective date
- 2023-12-11
- Source export date
- 2026-09-28
- Source partition
- 1
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0001-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/9c7783846d422acb0c9e59457606951c785a7d28cc631c8cc4839d0dc7c55f39/drug-label-0001-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 05:14:06
| 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 | Redken 5th Avenue NYC Scalp Relief Dandruff Control | openfda.brand_name | |
| generic name | PYRITHIONE ZINC | openfda.generic_name | |
| manufacturer name | L'Oreal USA Products Inc | openfda.manufacturer_name | |
| ndc | package | 49967-795-03 | openfda.package_ndc |
| ndc | package | 49967-795-02 | openfda.package_ndc |
| ndc | package | 49967-795-01 | openfda.package_ndc |
| ndc | product | 49967-795 | openfda.product_ndc |
| ndc11 | package | 49967079502 | derived:openfda.package_ndc |
| ndc11 | package | 49967079503 | derived:openfda.package_ndc |
| ndc11 | package | 49967079501 | derived:openfda.package_ndc |
| rxcui | 209884 | openfda.rxcui | |
| spl id | 099d44dc-eff9-47d9-b252-e9f633f0016b | id | |
| spl set id | 306a1ef4-e7ed-4c8c-877c-3c34d3e6d7b7 | set_id | |
| unii | R953O2RHZ5 | openfda.unii |
Warnings cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.