NDC11 69423056827
This exact 11-digit normalized identifier can correspond to more than one FDA hyphenation. FDA.report preserves the exact identifier and exposes every structurally valid candidate without guessing.
Possible FDA NDC forms#
| Package NDC | Product root |
|---|---|
| 69423-0568-27 | 69423-0568 |
| 69423-568-27 | 69423-568 |
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 |
|---|---|---|---|---|---|---|
| Head and Shoulders Clinical Dry Scalp Rescue Kit | PYRITHIONE ZINC | The Procter & Gamble Manufacturing Company | 1a3ac96a-04ec-6865-e063-6394a90a9fb8 | 2025-12-31 | Warnings | 69423-568-27 69423056827 |
| Head and Shoulders Clinical Dandruff Defense Dry Scalp Rescue | PYRITHIONE ZINC | The Procter & Gamble Manufacturing Company | c7bc3942-6943-2ea5-e053-2a95a90a42a9 | 2025-12-18 | Warnings | 69423-568-27 69423-568 69423056827 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.