NDC 55714-4293 - Parasites
This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.
- Product NDC
- 55714-4293
- Package NDCs from labels
- 55714-4293-1
- Manufacturer
- Newton Laboratories, Inc.
- Effective date
- 2019-01-14
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Parasites | Newton Laboratories, Inc. | 2019-01-14 | OTC ANIMAL DRUG LABEL |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 55714-4293 | PARASITES (ARTEMISIA ABROTANUM FLOWERING TOP, HORSE CHESTNUT, GARLIC, ARSENIC TRIOXIDE, ARTEMISIA VULGARIS ROOT, BAPTISIA TINCTORIA ROOT, ARTEMISIA CINA FLOWER, COPPER, DRYOPTERIS FILIX-MAS ROOT, PUNICA GRANATUM ROOT BARK, IPECAC, LACHESIS MUTA VENOM, LYCOPODIUM CLAVATUM SPORE, MERCURY, NAPHTHALENE, SODIUM CHLORIDE, STRYCHNOS NUX-VOMICA SEED, PULSATILLA VULGARIS, KRAMERIA LAPPACEA ROOT, RUTA GRAVEOLENS FLOWERING TOP, SCHOENOCAULON OFFICINALE SEED, SANTONIN, SILICON DIOXIDE, SPIGELIA ANTHELMIA, TURPENTINE OIL) LIQUID PARASITES (ARTEMISIA ABROTANUM FLOWERING TOP, HORSE CHESTNUT, GARLIC, ARSENIC TRIOXIDE, ARTEMISIA VULGARIS ROOT, BAPTISIA TINCTORIA ROOT, ARTEMISIA CINA FLOWER, COPPER, DRYOPTERIS FILIX-MAS ROOT, PUNICA GRANATUM ROOT BARK, IPECAC, LACHESIS MUTA VENOM, LYCOPODIUM CLAVATUM SPORE, MERCURY, NAPHTHALENE, SODIUM CHLORIDE, STRYCHNOS NUX-VOMICA SEED, PULSATILLA VULGARIS, KRAMERIA LAPPACEA ROOT, RUTA GRAVEOLENS FLOWERING TOP, SCHOENOCAULON OFFICINALE SEED, SANTONIN, SILICON DIOXIDE, SPIGELIA ANTHELMIA, TUR | 4 | Unmatched | 20191028_f48df69c-7287-5fb4-a609-edc0f45bac04.zip |
DailyMed Socrata Ingredients#
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.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.