Aconitum Napellus 200C
- Product NDC
- 43406-0159
- 11-digit product format
- 434060159
- Labeler code
- 43406
- Product ID
- 43406-0159_af011067-478f-4d5e-8e3f-d98864508175
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Aconitum Napellus
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Natural Creations, Inc
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2013-02-26
- Substance
- ACONITUM NAPELLUS
- 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
- Aconitum Napellus 200C
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ACONITUM NAPELLUS | 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 |
|---|
| 43406-0159-1 | Aconitum Napellus 200C | 30 mL in 1 BOTTLE, DROPPER | LIQUID | 30 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 43406-0159 | ACONITUM NAPELLUS 200C (ACONITUM NAPELLUS) LIQUID [NATURAL CREATIONS, INC] | 2 | Current NDC, Legacy NDC, 1 package rows | 20220215_91f429ad-10ef-45e0-b7f8-3c254d873cb5.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 43406-0159-1 | 43406015901 | 30 mL in 1 BOTTLE, DROPPER (43406-0159-1) | 30 ml | 2013-02-26 | 0000-00-00 | No | No | Current |