| NDC Code | 58264-0211-1 |
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| Package Description | 29.57 mL in 1 BOTTLE, GLASS (58264-0211-1) |
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| Product NDC | 58264-0211 |
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| Product Type Name | HUMAN OTC DRUG |
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| Proprietary Name | N-13 |
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| Non-Proprietary Name | Ceanothus Americanus Leaf, Urtica Urens, Sodium Chloride, Lachesis Muta Whole, Cinchona Officinalis Bark, Lycopodium Clavatum Whole, Ferric Chloride Hexahydrate, And Sus Scrofa Spleen |
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| Dosage Form | SOLUTION |
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| Usage | SUBLINGUAL |
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| Start Marketing Date | 19900101 |
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| Marketing Category Name | UNAPPROVED HOMEOPATHIC |
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| Manufacturer | DNA Labs, Inc. |
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| Substance Name | CEANOTHUS AMERICANUS LEAF; CINCHONA OFFICINALIS BARK; FERRIC CHLORIDE HEXAHYDRATE; LACHESIS MUTA WHOLE; LYCOPODIUM CLAVATUM WHOLE; SODIUM CHLORIDE; SUS SCROFA SPLEEN; URTICA URENS |
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| Strength | 4; 8; 6; 12; 6; 6; 200; 4 |
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| 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 |
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| Pharmacy Classes | Iron [CS], Parenteral Iron Replacement [EPC], Phosphate Binder [EPC], Phosphate Chelating Activity [MoA] |
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