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