NDC11 70163000301
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 |
|---|---|
| 70163-0003-01 | 70163-0003 |
| 70163-0003-1 | 70163-0003 |
| 70163-003-01 | 70163-003 |
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 |
|---|---|---|---|---|---|---|
| Ringstop | ACETYLSALICYLICUM ACIDUM, CALCAREA CARBONICA, CARBO VEGETABILIS, CHININUM SULPHURICUM, CIMICIFUGA RACEMOSA, CINCHONA OFFICINALIS, COFFEA CRUDA, GRAPHITES, KALI CARBONICUM, LYCOPODIUM CLAVATUM, NATRUM SALICYLICUM | NaturalCare | f6e3501d-1a27-462d-ab07-1b2d6fe91535 | 2026-03-02 | Warnings | 70163-0003-1 70163-0003 70163000301 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.