ACONITE
- Product NDC
- 44911-0209
- 11-digit product format
- 449110209
- Labeler code
- 44911
- Product ID
- 44911-0209_04259ae1-7e7d-4018-9866-9b0f378b2cfc
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Aconitum napellus
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- ENERGIQUE, INC.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2015-07-15
- Substance
- ACONITUM NAPELLUS WHOLE
- Active strength
- 200 [hp_C]/mL
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- ACONITE
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ACONITUM NAPELLUS WHOLE | 200 [hp_C]/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | U0NQ8555JD |
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 44911-0209-1 | ACONITE | 30 mL in 1 BOTTLE, DROPPER | LIQUID | 30 | | 4 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 44911-0209 | ACONITE (ACONITUM NAPELLUS) LIQUID [ENERGIQUE, INC.] | 4 | Current NDC, Legacy NDC, 1 package rows | 20230609_e5f8aa8c-0764-49e8-a2b1-4b8291eef882.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 44911-0209-1 | 44911020901 | 30 mL in 1 BOTTLE, DROPPER (44911-0209-1) | 30 ml | 2015-07-15 | 0000-00-00 | No | No | Current |