D-61 (tobacco leaf, salix nigra bark, camphor (natural), turpentine oil, berberis vulgaris root bark, solanum dulcamara whole, strychnos nux-vomica seed, rhododendron aureum leaf, and toxicodendron pubescens leaf)
**Product type:** Human Otc Drug
**Active ingredient:** BERBERIS VULGARIS ROOT BARK; CAMPHOR (NATURAL); RHODODENDRON AUREUM LEAF; SALIX NIGRA BARK; SOLANUM DULCAMARA WHOLE; STRYCHNOS NUX-VOMICA SEED; TOBACCO LEAF; TOXICODENDRON PUBESCENS LEAF; TURPENTINE OIL
**Strength:** 2; 6; 3; 3; 2; 2; 12; 3; 6 [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], Allergens [CS], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Increased IgG Production [PE], Non-Standardized Plant Allergenic Extract [EPC], Non-Standardized Plant Allergenic Extract [EPC], Plant Proteins [CS], Plant Proteins [CS], Seed Storage Proteins [CS]
/api/v1/systems/ndc_fda/nodes/58264-0061Hierarchy Explorer
Cross-system equivalences0
No cross-system equivalences mapped for this node.