Anxiety
- Product NDC
- 44911-0038
- Requested package NDC
- 44911-0038-1
- 11-digit product format
- 449110038
- Labeler code
- 44911
- Product ID
- 44911-0038_72b7dddf-c922-4dac-90ff-f7d5a07eebbd
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Aconitum Napellus, Arsenicum Album, Belladonna, Calcarea Carbonica, Carcinosin, Causticum, Gelsemium Sempervirens, Lachesis Mutus, Mercurius Vivus, Nitricum Acidum, Phosphorus, Rhus Tox
- Dosage form
- SPRAY
- Route
- ORAL
- Labeler
- Energique, Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2012-10-16
- Marketing end
- 0000-00-00
- Substance
- ARSENIC TRIOXIDE; ACONITUM NAPELLUS; ATROPA BELLADONNA; OYSTER SHELL CALCIUM CARBONATE, CRUDE; HUMAN BREAST TUMOR CELL; CAUSTICUM; GELSEMIUM SEMPERVIRENS ROOT; LACHESIS MUTA VENOM; MERCURY; NITRIC ACID; PHOSPHORUS; TOXICODENDRON PUBESCENS LEAF
- Active strength
- 30 [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
NDC auxiliary status#
These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.
| Dataset | Scope | Product NDC | Package NDC | Code | Status | Reporting period | Source date |
|---|---|---|---|---|---|---|---|
| excluded package | package | 44911-0038 | 44911-0038-1 | D | Discontinued by firm | 2026-10-12 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
DailyMed Product Concepts#
| Product concept | Relation | Version | Effective |
|---|---|---|---|
| 63f39a63-5cd1-4016-bd86-2bbb0f6c3139 | Product name | 3 | 20240506 |
| e5a77e9c-c528-733a-173d-914a234c024b | Product name | 5 | 20240506 |
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 44911-0038-1 | 2023-11-07 | C162847 | 48780-1 | f386c649-cf34-0266-e053-dadaa90a7c1a | Drug Facts: |
| 44911-0038-1 | 2023-01-30 | C162847 | 48780-1 | f386c649-cf34-0266-e053-dadaa90a7c1a | Drug Facts: |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 44911-0038-1 | Anxiety | 30 mL in 1 BOTTLE, SPRAY | SPRAY | 30 | 7 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 44911-0038 | ANXIETY (ACONITUM NAPELLUS, ARSENICUM ALBUM, BELLADONNA, CALCAREA CARBONICA, CARCINOSIN, CAUSTICUM, GELSEMIUM SEMPERVIRENS, LACHESIS MUTUS, MERCURIUS VIVUS, NITRICUM ACIDUM, PHOSPHORUS, RHUS TOX) SPRAY [ENERGIQUE, INC.] | 7 | Legacy NDC, 1 package rows | 20231108_c33e5a7b-249e-415b-8463-927dbca47e3a.zip |
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 44911-0038-1 | 44911003801 | 30 mL in 1 BOTTLE, SPRAY (44911-0038-1) | 30 ml | 2012-10-16 | 0000-00-00 | No | No | Current |