NDC11 70163003602
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 |
|---|---|
| 70163-0036-02 | 70163-0036 |
| 70163-0036-2 | 70163-0036 |
| 70163-036-02 | 70163-036 |
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 |
|---|---|---|---|---|---|---|
| Cough and Mucus | ANTIMONIUM TARTARICUM, EUPHRASIA OFFICINALIS, HEPAR SULPHURIS CALCAREUM, HYDRASTIS CANADENSIS, KALI BICHROMICUM, PULSATILLA (PRATENSIS), STANNUM METALLICUM, SULPHUR | NaturalCare | 5435e0ba-eef9-42a9-8301-aacacd2409b1 | 2026-03-23 | Warnings | 70163-0036-2 70163-0036 70163003602 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.