NDC11 53125070029
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 |
|---|---|
| 53125-0700-29 | 53125-0700 |
| 53125-700-29 | 53125-700 |
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 |
|---|---|---|---|---|---|---|
| North Woods Derma Foam Hand Sanitizer | BENZALKONIUM CHLORIDE | Superior Chemical Corporation | ad51a175-2b91-fd14-e053-2995a90ad54d | 2026-09-09 | Warnings | 53125-700-29 53125-700 53125070029 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.