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.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.