NDC11 70000042201
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 |
|---|---|
| 70000-0422-01 | 70000-0422 |
| 70000-0422-1 | 70000-0422 |
| 70000-422-01 | 70000-422 |
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 |
|---|---|---|---|---|---|---|
| MAXIMUM STRENGTH ANTACID | ALUMINUM HYDROXIDE, MAGNESIUM HYDROXIDE, SIMETHICONE | CARDINAL HEALTH | 7ee3618a-43c8-2ccc-e053-2a91aa0a8115 | 2023-11-07 | Warnings | 70000-0422-1 70000-0422 70000042201 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.