NDC 61571-448 - EquioPathics Travel Anxiety
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
- 61571-448
- Package NDCs from labels
- 61571-448-04
- Manufacturer
- HomeoPet, LLC | Speciality Pharma Manufacturing LLC
- Effective date
- 2020-12-02
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| PHOSPHORIC ACID - HomeoPet, LLC | Speciality Pharma Manufacturing LLC | HomeoPet, LLC | Speciality Pharma Manufacturing LLC | 2020-12-02 | OTC ANIMAL DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 61571-448-04 | EquioPathics Travel Anxiety | 120 mL in 1 BOTTLE, DROPPER | LIQUID | 120 | 6 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 61571-448 | EQUIOPATHICS TRAVEL ANXIETY (PHOSPHORICUM ACIDUM, IGNATIA AMARA, ZINCUM VALERIANICUM, KALI BROMATUM, SCUTELLARIA LATERIFLORA) LIQUID [HOMEOPET, LLC] | 6 | 1 package rows | 20201205_9b6b7c2a-4cf8-40fe-8736-540ebfe60aa8.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.
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Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.