NDC 44911-0685-01 - 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
- 44911-0685
- Requested NDC
- 44911-0685-01
- Package NDCs from labels
- 44911-0685-1, 44911-0685-01
- Manufacturer
- Energique, Inc. | Apotheca Company
- Effective date
- 2023-11-03
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Anxiety - Energique, Inc. | Apotheca Company | Energique, Inc. | Apotheca Company | 2023-11-03 | HUMAN OTC DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 44911-0685-1 | Anxiety | 30 mL in 1 BOTTLE, SPRAY | SPRAY | 30 | 1 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 44911-0685 | ANXIETY (ACONITUM NAPELLUS, ARGENTUM NITRICUM, ARSENICUM ALBUM, BELLADONNA, CALCAREA CARBONICA, CARCINOSIN, CAUSTICUM, GELSEMIUM SEMPERVIRENS, LACHESIS MUTUS, LITHIUM CARBONICUM, LYCOPODIUM CLAVATUM, MERCURIUS VIVUS, NITRICUM ACIDUM, PHOSPHORUS, RHUS TOX) SPRAY [ENERGIQUE, INC.] | 1 | Current NDC, 1 package rows | 20231104_2fd7051b-d274-4028-8348-b175a22f045c.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.