Aconitum napellus
- Product NDC
- 63083-7101
- 11-digit product format
- 630837101
- Labeler code
- 63083
- Product ID
- 63083-7101_4b2be726-84eb-4d52-be74-2955c6d83ffb
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Aconitum napellus
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Professional Complementary Health Formulas
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 1984-08-15
- Substance
- ACONITUM NAPELLUS WHOLE
- Active strength
- 6 [hp_X]/29.5mL
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Aconitum napellus
- Brand name suffix
- 7101
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ACONITUM NAPELLUS WHOLE | 6 [hp_X]/29.5mL |
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 |
|---|
| 63083-7101-1 | Aconitum napellus7101 | 29.5 mL in 1 BOTTLE, DROPPER | LIQUID | 29.5 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 63083-7101 | ACONITUM NAPELLUS 7101 (ACONITUM NAPELLUS) LIQUID [PROFESSIONAL COMPLEMENTARY HEALTH FORMULAS] | 1 | Current NDC, Legacy NDC, 1 package rows | 20220218_9d04cb5d-cafa-4a64-bd6e-5724b9ee36ef.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63083-7101-1 | 63083710101 | 29.5 mL in 1 BOTTLE, DROPPER (63083-7101-1) | 29.5 ml | 1985-08-15 | 0000-00-00 | No | No | Current |