Artemisia vulgaris
- Product NDC
- 0220-0606
- 11-digit product format
- 002200606
- Labeler code
- 0220
- Product ID
- 0220-0606_253c9d92-7556-4429-e063-6394a90a52f1
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- ARTEMISIA VULGARIS ROOT
- Dosage form
- PELLET
- Route
- ORAL
- Labeler
- Boiron
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2024-01-01
- Substance
- ARTEMISIA VULGARIS ROOT
- Active strength
- 200 [kp_C]/200[kp_C]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 0220-0606-41 | Artemisia vulgaris | 200 [kp_C] in 1 TUBE | PELLET | 200 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 0220-0606 | ARTEMISIA VULGARIS (ARTEMISIA VULGARIS ROOT) PELLET [BOIRON] | 1 | Current NDC, 1 package rows | 20241027_253c9d92-7555-4429-e063-6394a90a52f1.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 0220-0606-41 | 00220060641 | 200 [kp_C] in 1 TUBE (0220-0606-41) | 2024-01-01 | No | No | Historical |