NDC 61571-601 - Digestive Upsets
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
- 61571-601
- Package NDCs from labels
- 61571-601-15
- Manufacturer
- HomeoPet, LLC | Speciality Pharma Manufacturing LLC
- Effective date
- 2020-11-17
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Digestive Upsets - HomeoPet, LLC | Speciality Pharma Manufacturing LLC | HomeoPet, LLC | Speciality Pharma Manufacturing LLC | 2020-11-17 | OTC ANIMAL DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 61571-601-15 | Digestive Upsets | 15 mL in 1 BOTTLE, DROPPER | LIQUID | 15 | 2 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 61571-601 | DIGESTIVE UPSETS (ACONITUM NAP, ALOE, ARSENICUM ALB, PHOS, CARBO VEG, CHELIDONIUM MA, CHININUM PU, IPECAC, PHOSPHORICUM AC, PODOPH PELT, VERATRUM AL, LYCOPODIUM, MERC SOLUB, NUX VOM, SULPH) LIQUID [HOMEOPET, LLC] | 2 | 1 package rows | 20201205_2924d3ec-d65d-4b3e-a90d-569fec24aa61.zip |
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.
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Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.