B Mold Mixture is a Intradermal; Subcutaneous Injection, Solution in the Human Prescription Drug category. It is labeled and distributed by Antigen Laboratories, Inc.. The primary component is Trichothecium Roseum; Passalora Fulva; Cochliobolus Spicifer; Myrothecium Verrucaria; Hypomyces Perniciosus; Neurospora Crassa; Khuskia Oryzae; Paecilomyces Variotii; Microascus Brevicaulis; Colletotrichum Coccodes; Pleospora Herbarum; Streptomyces Griseus; Trichoderma Viride; Trichophyton Schoenleinii.
| Product ID | 49288-0037_272c9910-2160-4d41-afbd-faab3055ba1d | 
| NDC | 49288-0037 | 
| Product Type | Human Prescription Drug | 
| Proprietary Name | B Mold Mixture | 
| Generic Name | B Mold Mixture | 
| Dosage Form | Injection, Solution | 
| Route of Administration | INTRADERMAL; SUBCUTANEOUS | 
| Marketing Start Date | 1974-03-23 | 
| Marketing Category | BLA / BLA | 
| Application Number | BLA102223 | 
| Labeler Name | Antigen Laboratories, Inc. | 
| Substance Name | TRICHOTHECIUM ROSEUM; PASSALORA FULVA; COCHLIOBOLUS SPICIFER; MYROTHECIUM VERRUCARIA; HYPOMYCES PERNICIOSUS; NEUROSPORA CRASSA; KHUSKIA ORYZAE; PAECILOMYCES VARIOTII; MICROASCUS BREVICAULIS; COLLETOTRICHUM COCCODES; PLEOSPORA HERBARUM; STREPTOMYCES GRISEUS; TRICHODERMA VIRIDE; TRICHOPHYTON SCHOENLEINII | 
| Active Ingredient Strength | 0 g/mL; g/mL; g/mL; g/mL; g/mL; g/mL; g/mL; g/mL; g/mL; g/mL; g/mL; g/mL; g/mL; g/mL | 
| Pharm Classes | Non-Standardized Fungal Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Increased IgG Production [PE],Fungal Proteins [CS],Allergens [CS],Non-Standardized Fungal Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Increased IgG Production [PE],Fungal Proteins [CS],Allergens [CS],Non-Standardized Fungal Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Increased IgG Production [PE],Fungal Proteins [CS],Allergens [CS],Non-Standardized Fungal Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Increased IgG Production [PE],Fungal Proteins [CS],Allergens [CS],Non-Standardized Fungal Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Increased IgG Production [PE],Fungal Proteins [CS],Allergens [CS],Non-Standardized Fungal Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Increased IgG Production [PE],Fungal Proteins [CS],Allergens [CS],Non-Standardized Fungal Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Increased IgG Production [PE],Fungal Proteins [CS],Allergens [CS],Non-Standardized Fungal Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Increased IgG Production [PE],Fungal Proteins [CS],Allergens [CS],Non-Standardized Fungal Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Increased IgG Production [PE],Fungal Proteins [CS],Allergens [CS],Non-Standardized Fungal Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Increased IgG Production [PE],Fungal Proteins [CS],Allergens [CS],Non-Standardized Bacterial Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Increased IgG Production [PE],Bacterial Proteins [CS],Allergens [CS],Fungal Proteins [CS],Allergens [CS],Non-Standardized Fungal Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Increased IgG Production [PE],Non-Standardized Fungal Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Increased IgG Production [PE],Fungal Proteins [CS],Allergens [CS] | 
| NDC Exclude Flag | E | 
| Listing Certified Through | 2017-12-31 | 
| Marketing Start Date | 1974-03-23 | 
| NDC Exclude Flag | N | 
| Sample Package? | N | 
| Marketing Category | BLA | 
| Application Number | BLA102223 | 
| Product Type | HUMAN PRESCRIPTION DRUG | 
| Marketing Start Date | 1974-03-23 | 
| Inactivation Date | 2019-10-21 | 
| Marketing Category | BLA | 
| Application Number | BLA102223 | 
| Product Type | HUMAN PRESCRIPTION DRUG | 
| Marketing Start Date | 1974-03-23 | 
| Inactivation Date | 2019-10-21 | 
| Marketing Category | BLA | 
| Application Number | BLA102223 | 
| Product Type | HUMAN PRESCRIPTION DRUG | 
| Marketing Start Date | 1974-03-23 | 
| Inactivation Date | 2019-10-21 | 
| Marketing Category | BLA | 
| Application Number | BLA102223 | 
| Product Type | HUMAN PRESCRIPTION DRUG | 
| Marketing Start Date | 1974-03-23 | 
| Inactivation Date | 2019-10-21 | 
| Marketing Category | BLA | 
| Application Number | BLA102223 | 
| Product Type | HUMAN PRESCRIPTION DRUG | 
| Marketing Start Date | 1974-03-23 | 
| Inactivation Date | 2019-10-21 | 
| Ingredient | Strength | 
|---|---|
| TRICHOTHECIUM ROSEUM | .0018 g/mL | 
| SPL SET ID: | 6d2006e2-55ea-41db-bd17-ce6d080f28a0 | 
| Manufacturer | |
| UNII | 
 | 
| RxNorm Concept Unique ID - RxCUI | |
| Pharm Class PE | |
| PHarm Class EPC | |
| NUI Code | 
| NDC | Brand Name | Generic Name | 
|---|---|---|
| 49288-0035 | B Mold Mixture | B Mold Mixture | 
| 49288-0036 | B Mold Mixture | B Mold Mixture | 
| 49288-0037 | B Mold Mixture | B Mold Mixture |