NDC11 70558000901
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 |
|---|---|
| 70558-0009-01 | 70558-0009 |
| 70558-0009-1 | 70558-0009 |
| 70558-009-01 | 70558-009 |
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 |
|---|---|---|---|---|---|---|
| Thyro Support | SARCOLACTICUM ACIDUM, VISCUM ALBUM, IODIUM, FUCUS VESICULOSUS, GALIUM APARINE, NATRUM OXALACETICUM, THYROIDINUM (SUIS), DHEA (DEHYDROEPIANDROSTERONE), PHENYL ISOTHIOCYANATE, TYRAMINE, ADENOSINUM TRIPHOSPHORICUM DINATRUM, ALPHA-KETOGLUTARICUM ACIDUM, FUMARICUM ACIDUM, MALICUM ACID, COLCHICUM AUTUMNALE, CONIUM MACULATUM, FUNICULUS UMBILICALIS SUIS, HEPAR SUIS, MEDULLA OSSIS SUIS, PINEAL GLAND (SUIS), SPLEEN (SUIS), THYMUS (SUIS), CALCAREA FLUORICA, PULSATILLA (PRATENSIS), SPONGIA TOSTA, CORTISONE ACETICUM, | Pro Weight Loss Inc. | 171e9798-35ac-498b-944e-0173c46188d7 | 2025-01-08 | Warnings | 70558-0009-1 70558-0009 70558000901 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.