World Of Taxonomy
58264-0037Level 3

D-37 (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)

**Product type:** Human Otc Drug

**Active ingredient:** 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 [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

**Dosage form:** Solution

**Route:** Sublingual

**Labeler:** DNA Labs, Inc.

**Marketing category:** UNAPPROVED HOMEOPATHIC

**Pharmacologic class:** 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]

GET/api/v1/systems/ndc_fda/nodes/58264-0037
Official DownloadPublic Domain (US Government)Source

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