warnings
Warnings For external use only
Dry Scalp Care
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
- Dry Scalp Care
- Generic name
- PYRITHIONE ZINC
- Manufacturer
- The Kroger Co.
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 837d7a14-b312-4dce-a00a-623b50329378
- SPL ID
- 4bd0ba1e-8117-760f-e063-6294a90a46a9
- Version
- 18
- Effective date
- 2026-02-27
- Source export date
- 2026-10-12
- 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/2026-10-12/7928c8e8c6256620071a8b7e5b93eb8dfa543649c08d17a01ea02251012ba58c/drug-label-0001-of-0014.json.zip
- Source manifest SHA-256
- 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
- Import run
- 20261013T011858Z
- Imported at
- 2026-10-13 01:25:08
| 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 | Dry Scalp Care | openfda.brand_name | |
| generic name | PYRITHIONE ZINC | openfda.generic_name | |
| manufacturer name | The Kroger Co. | openfda.manufacturer_name | |
| ndc | package | 30142-296-15 | openfda.package_ndc |
| ndc | package | 30142-296-35 | openfda.package_ndc |
| ndc | package | 30142-296-32 | openfda.package_ndc |
| ndc | package | 30142-296-40 | openfda.package_ndc |
| ndc | product | 30142-296 | openfda.product_ndc |
| ndc11 | package | 30142029615 | derived:openfda.package_ndc |
| ndc11 | package | 30142029635 | derived:openfda.package_ndc |
| ndc11 | package | 30142029632 | derived:openfda.package_ndc |
| ndc11 | package | 30142029640 | derived:openfda.package_ndc |
| rxcui | 209884 | openfda.rxcui | |
| spl id | 4bd0ba1e-8117-760f-e063-6294a90a46a9 | id | |
| spl set id | 837d7a14-b312-4dce-a00a-623b50329378 | 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 reaction Kroger DISTRIBUTED BY THE KROGER CO., CINCINNATI, OH 45202 QUESTIONS OR COMMENTS WWW.KROGER.COM PLEASE RECYCLE
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.