58264-0040Level 3
D-40 (PHOSPHORIC ACID, LYCOPODIUM CLAVATUM SPORE, SODIUM SULFATE, CLAVICEPS PURPUREA SCLEROTIUM, URANYL NITRATE HEXAHYDRATE, PHASEOLUS VULGARIS WHOLE, and ARSENIC TRIOXIDE)
**Product type:** Human Otc Drug
**Active ingredient:** ARSENIC TRIOXIDE; CLAVICEPS PURPUREA SCLEROTIUM; LYCOPODIUM CLAVATUM SPORE; PHASEOLUS VULGARIS WHOLE; PHOSPHORIC ACID; SODIUM SULFATE; URANYL NITRATE HEXAHYDRATE
**Strength:** 8; 4; 30; 12; 12; 12; 30 [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
GET
/api/v1/systems/ndc_fda/nodes/58264-0040Hierarchy Explorer
Loading...
Cross-system equivalences0
No cross-system equivalences mapped for this node.