Dock-Sorrel Mix is a Intradermal; Percutaneous; Subcutaneous Solution in the Non-standardized Allergenic category. It is labeled and distributed by Greer Laboratories, Inc.. The primary component is Rumex Acetosella Pollen; Rumex Crispus Pollen.
| Product ID | 22840-9317_7b43b65a-bbff-133f-e053-2991aa0a3395 |
| NDC | 22840-9317 |
| Product Type | Non-standardized Allergenic |
| Proprietary Name | Dock-Sorrel Mix |
| Generic Name | Rumex Acetosella And Rumex Crispus |
| Dosage Form | Solution |
| Route of Administration | INTRADERMAL; PERCUTANEOUS; SUBCUTANEOUS |
| Marketing Start Date | 1981-09-15 |
| Marketing Category | BLA / BLA |
| Application Number | BLA101833 |
| Labeler Name | Greer Laboratories, Inc. |
| Substance Name | RUMEX ACETOSELLA POLLEN; RUMEX CRISPUS POLLEN |
| Active Ingredient Strength | 0 g/mL; g/mL |
| Pharm Classes | Non-Standardized Pollen Allergenic Extract [EPC],Cell-mediated Immunity [PE],Increased IgG Production [PE],Pollen [CS],Increased Histamine Release [PE],Allergens [CS],Non-Standardized Pollen Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Increased IgG Production [PE],Pollen [CS],Allergens [CS] |
| NDC Exclude Flag | N |
| Listing Certified Through | 2019-12-31 |
| Marketing Start Date | 1981-09-15 |
| NDC Exclude Flag | N |
| Sample Package? | N |
| Marketing Category | BLA |
| Application Number | BLA101833 |
| Product Type | NON-STANDARDIZED ALLERGENIC |
| Marketing Start Date | 1981-09-15 |
| Ingredient | Strength |
|---|---|
| RUMEX ACETOSELLA POLLEN | .0005 g/mL |
| NDC | Brand Name | Generic Name |
|---|---|---|
| 22840-9315 | Dock-Sorrel Mix | Rumex acetosella and Rumex crispus |
| 22840-9316 | Dock-Sorrel Mix | Rumex acetosella and Rumex crispus |
| 22840-9317 | Dock-Sorrel Mix | Rumex acetosella and Rumex crispus |
| 22840-9319 | Dock-Sorrel Mix | Rumex acetosella and Rumex crispus |
| 0268-1302 | SORREL/DOCK MIX | RUMEX ACETOSELLA and RUMEX CRISPUS |