NDC11 70707021215
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 |
|---|---|
| 70707-0212-15 | 70707-0212 |
| 70707-212-15 | 70707-212 |
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 |
|---|---|---|---|---|---|---|
| Acne Med 10% | BENZOYL PEROXIDE | Face Reality, LLC | 45ad7429-ccd0-28f6-e054-00144ff88e88 | 2023-12-15 | Warnings | 70707-212-15 70707-212 70707021215 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.