PAEONIA OFFICINALIS
- Product NDC
- 0220-3897
- 11-digit product format
- 002203897
- Labeler code
- 0220
- Product ID
- 0220-3897_3a9d4dc4-cd80-586b-e063-6394a90a0eaa
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- PAEONIA OFFICINALIS ROOT
- Dosage form
- PELLET
- Route
- ORAL
- Labeler
- Boiron
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2025-01-01
- Substance
- PAEONIA OFFICINALIS 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 |
|---|
| 8R564U2E1P | PAEONIA OFFICINALIS ROOT | PAEONIA OFFICINALIS ROOT |
Packages
| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 0220-3897-41 | 00220389741 | 200 [kp_C] in 1 TUBE (0220-3897-41) | 2025-01-01 | No | No | Historical |