NDC11 69842017168
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 |
|---|---|
| 69842-0171-68 | 69842-0171 |
| 69842-171-68 | 69842-171 |
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 |
|---|---|---|---|---|---|---|
| Ultra Strength Antacid | CALCIUM ANTACID | CVS | 51acc196-ab1f-49ea-8a59-f06309f1953b | 2017-08-09 | Warnings | 69842-171-68 69842-171 69842017168 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.