NDC11 00067814202
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 |
|---|---|
| 00067-8142-02 | 00067-8142 |
| 00067-8142-2 | 00067-8142 |
| 0067-8142-02 | 0067-8142 |
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 |
|---|---|---|---|---|---|---|
| EX-LAX MAXIMUM STRENGTH STIMULANT LAXATIVE | SENNOSIDES | Haleon US Holdings LLC | fb170340-c996-46cf-b165-84e136ba4151 | 2024-12-17 | Warnings | 0067-8142-02 0067-8142 00067814202 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.