Trillium pendulum
- Product NDC
- 0220-5049
- 11-digit product format
- 002205049
- Labeler code
- 0220
- Product ID
- 0220-5049_00edbc51-9a8b-566f-e063-6294a90a81a7
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- TRILLIUM ERECTUM ROOT
- Dosage form
- PELLET
- Route
- ORAL
- Labeler
- Boiron
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 1983-03-03
- Substance
- TRILLIUM ERECTUM ROOT
- Active strength
- 9 [hp_C]/9[hp_C]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Matched term |
|---|
| AHW6F0T2X0 | TRILLIUM ERECTUM ROOT | TRILLIUM ERECTUM ROOT |
Packages
| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 0220-5049-41 | 00220504941 | 9 [hp_C] in 1 TUBE (0220-5049-41) | 1983-03-03 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Trillium pendulum 9C | Boiron | Boiron, Inc. | 2023-07-20 | HUMAN OTC DRUG LABEL | 3 |