GLYCYRRHIZA GLABRA
- Product NDC
- 0220-2305
- 11-digit product format
- 002202305
- Labeler code
- 0220
- Product ID
- 0220-2305_0a0d5748-6ceb-0f47-e063-6294a90a154e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- GLYCYRRHIZA GLABRA
- Dosage form
- PELLET
- Route
- ORAL
- Labeler
- Boiron
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 1983-03-03
- Substance
- GLYCYRRHIZA GLABRA
- Active strength
- 30 [hp_C]/30[hp_C]
- Pharmacologic classes
- Allergens [CS], Cell-mediated Immunity [PE], Dietary Proteins [CS], Increased Histamine Release [PE], Non-Standardized Food Allergenic Extract [EPC], Non-Standardized Plant Allergenic Extract [EPC], Plant Proteins [CS]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 2788Z9758H | GLYCYRRHIZA GLABRA | 84775-66-6 | GLYCYRRHIZA GLABRA |
Packages
| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 0220-2305-41 | 00220230541 | 30 [hp_C] in 1 TUBE (0220-2305-41) | 1983-03-03 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Glycyrrhiza glabra 30C | Boiron | Boiron, Inc. | 2023-11-13 | HUMAN PRESCRIPTION DRUG LABEL | 3 |