Aconitum 30X
- Product NDC
- 53645-1612
- 11-digit product format
- 536451612
- Labeler code
- 53645
- Product ID
- 53645-1612_1e8f8326-67f3-d782-e063-6394a90af343
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Aconitum 30X
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- True Botanica, LLC
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2024-10-07
- Substance
- ACONITUM NAPELLUS ROOT
- Active strength
- 30 [hp_X]/30mL
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Aconitum 30X
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ACONITUM NAPELLUS ROOT | 30 [hp_X]/30mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | KPD2N7348X |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 53645-1612-6 | Aconitum 30X | 30 mL in 1 BOTTLE | LIQUID | 30 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 53645-1612 | ACONITUM 30X LIQUID [TRUE BOTANICA, LLC] | 1 | Current NDC, 1 package rows | 20241010_1e8f6f50-6140-a852-e063-6394a90a53d7.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 53645-1612-6 | 53645161206 | 30 mL in 1 BOTTLE (53645-1612-6) | 30 ml | 2024-10-07 | No | No | Current |