GRATIOLA OFFICINALIS
- Product NDC
- 0220-2330
- 11-digit product format
- 002202330
- Labeler code
- 0220
- Product ID
- 0220-2330_3a750f92-d3e8-640f-e063-6294a90a73f0
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- GRATIOLA OFFICINALIS WHOLE
- Dosage form
- PELLET
- Route
- ORAL
- Labeler
- Boiron
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2025-01-01
- Substance
- GRATIOLA OFFICINALIS
- 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 |
|---|
| BDD9991A36 | GRATIOLA OFFICINALIS | GRATIOLA OFFICINALIS |
Packages
| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 0220-2330-41 | 00220233041 | 200 [kp_C] in 1 TUBE (0220-2330-41) | 2025-01-01 | No | No | Historical |