| Product ID | 58264-0211_e0cfdec7-78f8-ad59-e053-2a95a90afea8 |
| NDC | 58264-0211 |
| Product Type | Human Otc Drug |
| Proprietary Name | N-13 |
| Generic Name | Ceanothus Americanus Leaf, Urtica Urens, Sodium Chloride, Lachesis Muta Whole, Cinchona Officinalis Bark, Lycopodium Clavatum Whole, Ferric Chloride Hexahydrate, And Sus Scrofa Spleen |
| Dosage Form | Solution |
| Route of Administration | SUBLINGUAL |
| Marketing Start Date | 1990-01-01 |
| Marketing Category | UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC |
| Labeler Name | DNA Labs, Inc. |
| Substance Name | CEANOTHUS AMERICANUS LEAF; CINCHONA OFFICINALIS BARK; FERRIC CHLORIDE HEXAHYDRATE; LACHESIS MUTA WHOLE; LYCOPODIUM CLAVATUM WHOLE; SODIUM CHLORIDE; SUS SCROFA SPLEEN; URTICA URENS |
| Active Ingredient Strength | 4 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL |
| Pharm Classes | Iron [CS], Parenteral Iron Replacement [EPC], Phosphate Binder [EPC], Phosphate Chelating Activity [MoA] |
| NDC Exclude Flag | N |
| Listing Certified Through | 2023-12-31 |