NDC11 53329018176
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 |
|---|---|
| 53329-0181-76 | 53329-0181 |
| 53329-181-76 | 53329-181 |
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 |
|---|---|---|---|---|---|---|
| ReadyBath Luxe | BENZALKONIUM CHLORIDE | Medline Industries, LP | 33376694-fccd-6ed5-e054-00144ff8d46c | 2025-06-11 | Warnings | 53329-181-76 53329-181 53329018176 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.