| NDC Code | 58264-0037-1 |
| Package Description | 29.57 mL in 1 BOTTLE, GLASS (58264-0037-1) |
| Product NDC | 58264-0037 |
| Product Type Name | HUMAN OTC DRUG |
| Proprietary Name | D-37 |
| Non-Proprietary Name | Aluminum Oxide, Bryonia Alba Root, Citrullus Colocynthis Fruit Pulp, Lachesis Muta Venom, Lycopodium Clavatum Spore, Mercuric Chloride, Strychnos Nux-vomica Seed, Lead Acetate Anhydrous, And Sulfur |
| Dosage Form | SOLUTION |
| Usage | SUBLINGUAL |
| Start Marketing Date | 19900101 |
| Marketing Category Name | UNAPPROVED HOMEOPATHIC |
| Manufacturer | DNA Labs, Inc. |
| Substance Name | ALUMINUM OXIDE; BRYONIA ALBA ROOT; CITRULLUS COLOCYNTHIS FRUIT PULP; LACHESIS MUTA VENOM; LEAD ACETATE ANHYDROUS; LYCOPODIUM CLAVATUM SPORE; MERCURIC CHLORIDE; STRYCHNOS NUX-VOMICA SEED; SULFUR |
| Strength | 12; 4; 4; 30; 12; 4; 8; 6; 12 |
| Strength Unit | [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL |
| Pharmacy Classes | Allergens [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Non-Standardized Plant Allergenic Extract [EPC], Plant Proteins [CS], Seed Storage Proteins [CS] |