AB
- Product NDC
- 60986-2040
- 11-digit product format
- 609862040
- Labeler code
- 60986
- Product ID
- 60986-2040_483ad8b7-56c6-1dc3-e063-6394a90abb23
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- ACONITUM NAPELLUS, BRYONIA CRETICA
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- MARCO PHARMA INTERNATIONAL LLC
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2025-02-06
- Substance
- ACONITUM NAPELLUS; BRYONIA CRETICA SUBSP. DIOICA ROOT
- Active strength
- 3; 3 [hp_X]/100mL; [hp_X]/100mL
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- AB
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ACONITUM NAPELLUS | 3 [hp_X]/100mL |
| BRYONIA CRETICA SUBSP. DIOICA ROOT | 3 [hp_X]/100mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | U0NQ8555JD, 53UB5FH7CX |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 60986-2040-3 | AB | 50 mL in 1 BOTTLE | LIQUID | 50 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 60986-2040 | AB (ACONITUM NAPELLUS, BRYONIA CRETICA) LIQUID [MARCO PHARMA INTERNATIONAL LLC] | 1 | Current NDC, 1 package rows | 20250209_2d81c13f-102a-6741-e063-6294a90aee84.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 60986-2040-3 | 60986204003 | 50 mL in 1 BOTTLE (60986-2040-3) | 50 ml | 2025-02-06 | No | No | Historical |