58264-0211Level 3
N-13 (Ceanothus americanus leaf, Urtica urens, Sodium Chloride, Lachesis muta whole, Cinchona officinalis Bark, Lycopodium clavatum Whole, Ferric chloride hexahydrate, and Sus scrofa spleen)
**Product type:** Human Otc Drug
**Active ingredient:** CEANOTHUS AMERICANUS LEAF; CINCHONA OFFICINALIS BARK; FERRIC CHLORIDE HEXAHYDRATE; LACHESIS MUTA WHOLE; LYCOPODIUM CLAVATUM WHOLE; SODIUM CHLORIDE; SUS SCROFA SPLEEN; URTICA URENS
**Strength:** 4; 8; 6; 12; 6; 6; 200; 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
**Dosage form:** Solution
**Route:** Sublingual
**Labeler:** DNA Labs, Inc.
**Marketing category:** UNAPPROVED HOMEOPATHIC
**Pharmacologic class:** Iron [CS], Parenteral Iron Replacement [EPC], Phosphate Binder [EPC], Phosphate Chelating Activity [MoA]
GET
/api/v1/systems/ndc_fda/nodes/58264-0211Hierarchy Explorer
Loading...
Cross-system equivalences0
No cross-system equivalences mapped for this node.