NDC11 69693071512
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 |
|---|---|
| 69693-0715-12 | 69693-0715 |
| 69693-715-12 | 69693-715 |
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 |
|---|---|---|---|---|---|---|
| CERTAIN DRI ROLL-ON | ALUMINUM CHLORIDE | Clarion Brands, LLC | 24282949-5c38-d3fb-adbe-f5c699f87d73 | 2025-12-23 | Warnings | 69693-715-12 69693-715 69693071512 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.