Lymph Stim Liquescence

NDC 63083-3016 · Professional Complementary Health Formulas

Generic nameLymph Stim Liquescence

Dosage formLIQUID

RouteORAL

Active ingredient(s)SCROPHULARIA NODOSA WHOLE, ECHINACEA ANGUSTIFOLIA WHOLE, ECHINACEA PURPUREA WHOLE, LEMON JUICE, SILICON DIOXIDE, PHYTOLACCA AMERICANA ROOT, THUJA OCCIDENTALIS LEAF, CAPSICUM, GOLDENSEAL, BOS TAURUS LYMPH VESSEL, SUS SCROFA MAMMARY GLAND, BOS TAURUS SPLEEN, HYSSOPUS OFFICINALIS WHOLE, ARSENIC TRIIODIDE, LACHESIS MUTA VENOM

Strength12; 6; 6; 6; 2; 2; 6; 6; 12; 3; 4; 1; 3; 6; 4 [hp_X]/118mL; [hp_X]/118mL; [hp_X]/118mL; [hp_X]/118mL; [hp_X]/118mL; [hp_X]/118mL; [hp_X]/118mL; [hp_X]/118mL; [hp_X]/118mL; [hp_X]/118mL; [hp_X]/118mL; [hp_X]/118mL; [hp_X]/118mL; [hp_X]/118mL; [hp_X]/118mL

Pharmacologic classAllergens [CS], Cell-mediated Immunity [PE], Dietary Proteins [CS], Increased Histamine Release [PE], Non-Standardized Food Allergenic Extract [EPC], Non-Standardized Plant Allergenic Extract [EPC], Plant Proteins [CS], Vegetable Proteins [CS]

Marketing categoryUNAPPROVED HOMEOPATHIC

Packages

63083-3016-4 — 118 mL in 1 BOTTLE, DROPPER (63083-3016-4)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

63083-2171 — Difficulty Breathing Drops, 63083-2174 — Fertility Drops, 63083-2175 — Rehydration Drops, 63083-3004 — Blood Stim Liquescence, 63083-3005 — Bone Stim Liquescence, 63083-3007 — Digestive Enzyme Liquescence, 63083-3008 — Turskas Liquescence, 63083-3009 — Female Balance Liquescence, 63083-3013 — Kidney Stim Liquescence, 63083-3015 — Liver Stim Liquescence, 63083-3017 — Mucolytic Drainage Liquescence, 63083-3020 — Cartilage Liquescence, 63083-3022 — C-Balance Liquescence, 63083-3023 — Spleen Thymus Liquescence, 63083-3024 — Connective Tissue Liquescence, 63083-3025 — Degex Liquescence, 63083-3027 — Skin Balance Liquescence, 63083-3028 — Spleen Stim Liquescence, 63083-3029 — Immune Enhancement Liquescence, 63083-3031 — Allergy Liquescence, +1771 more

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