Solvent/Small Ring Combination

NDC 63083-9317 · Professional Complementary Health Formulas

Generic nameSolvent/Small Ring Combination

Dosage formLIQUID

RouteORAL

Active ingredient(s)BLACK COHOSH, GELSEMIUM SEMPERVIRENS ROOT, STRYCHNOS NUX-VOMICA SEED, BERBERIS VULGARIS ROOT BARK, CHELIDONIUM MAJUS WHOLE, ANILINE, CYCLOHEXANOL, ESTRADIOL BENZOATE, MERCURIC CATION, TOLUENE, MUSK XYLENE, BENZENE

Strength12; 14; 10; 3; 10; 12; 12; 3; 12; 12; 6; 12 [hp_X]/29.5mL; [hp_X]/29.5mL; [hp_X]/29.5mL; [hp_X]/29.5mL; [hp_X]/29.5mL; [hp_X]/29.5mL; [hp_X]/29.5mL; [hp_X]/29.5mL; [hp_X]/29.5mL; [hp_X]/29.5mL; [hp_X]/29.5mL; [hp_X]/29.5mL

Pharmacologic classAllergens [CS], Cell-mediated Immunity [PE], Estradiol Congeners [CS], Estrogen Receptor Agonists [MoA], Estrogen [EPC], Increased Histamine Release [PE], Increased IgG Production [PE], Non-Standardized Plant Allergenic Extract [EPC], Plant Proteins [CS], Seed Storage Proteins [CS]

Marketing categoryUNAPPROVED HOMEOPATHIC

Packages

63083-9317-1 — 29.5 mL in 1 BOTTLE, DROPPER (63083-9317-1)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

63083-9306 — Thio Combination, 63083-9307 — Uric Acid Combination, 63083-9309 — Organophosphate Combination, 63083-9310 — Nitrogen Combination, 63083-9311 — Bridged Ring Combination, 63083-9312 — Bridged Phenyl Combination, 63083-9313 — Bridged Chlorinated Ring Combination, 63083-9314 — Chlorinated Ring Combination, 63083-9315 — Simple Chlorinated Combination, 63083-9316 — Peroxide Combination, 63083-9318 — Nitro-Thio Combination, 63083-9319 — Bile Acids Combination, 63083-9407 — Domestic Animals Nosode Combination, 63083-9408 — Childhood Diseases Nosode Combination, 63083-9410 — Urinary Nosode Combination, 63083-9411 — Intestinal Nosode Combination, 63083-9412 — Normal Intestinal Flora Nosode Combination, 63083-9414 — Pneumonia/Meningitis Nosode Combination, 63083-9415 — Proteus Nosode Combination, 63083-9416 — Soil/Water Contaminants Nosode Combination, +1324 more

From the FDA National Drug Code Directory, retrieved 2026-08-24. Product listings are submitted by labelers; FDA does not verify them.