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
Related UNII Ingredients
| UNII | Preferred term | Matched term |
|---|
| 32MP823R8S | ARTEMISIA VULGARIS ROOT | ARTEMISIA VULGARIS ROOT |
Packages
| 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 |