NDC 63083-9219

Clematis Combination 9219

Clematis Combination

Clematis Combination 9219 is a Oral Liquid in the Human Otc Drug category. It is labeled and distributed by Professional Complementary Health Formulas. The primary component is Apis Mellifera; Betula Pubescens Whole; Calcium Fluoride; Caltha Palustris Whole; Clematis Recta Flowering Top; Echinacea Angustifolia Whole; Galium Aparine Whole; Hedera Helix Flowering Twig; Juniperus Communis Var. Saxatilis Whole; Nitric Acid; Ononis Repens Whole; Phosphorus; Quillaja Saponaria Wood; Rancid Beef; Sedum Acre Whole; Sempervivum Tectorum Leaf; Silver; Thuja Occidentalis Leaf; Urtica Urens Whole.

Product ID63083-9219_87f940b9-5673-4265-a4ca-1f8362d21871
NDC63083-9219
Product TypeHuman Otc Drug
Proprietary NameClematis Combination 9219
Generic NameClematis Combination
Dosage FormLiquid
Route of AdministrationORAL
Marketing Start Date1984-08-15
Marketing CategoryUNAPPROVED HOMEOPATHIC /
Labeler NameProfessional Complementary Health Formulas
Substance NameAPIS MELLIFERA; BETULA PUBESCENS WHOLE; CALCIUM FLUORIDE; CALTHA PALUSTRIS WHOLE; CLEMATIS RECTA FLOWERING TOP; ECHINACEA ANGUSTIFOLIA WHOLE; GALIUM APARINE WHOLE; HEDERA HELIX FLOWERING TWIG; JUNIPERUS COMMUNIS VAR. SAXATILIS WHOLE; NITRIC ACID; ONONIS REPENS WHOLE; PHOSPHORUS; QUILLAJA SAPONARIA WOOD; RANCID BEEF; SEDUM ACRE WHOLE; SEMPERVIVUM TECTORUM LEAF; SILVER; THUJA OCCIDENTALIS LEAF; URTICA URENS WHOLE
Active Ingredient Strength12 [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; [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
Pharm ClassesAllergens [CS], Bee Venoms [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Standardized Insect Venom Allergenic Extract [EPC]
NDC Exclude FlagN
Listing Certified Through2023-12-31

Packaging

NDC 63083-9219-1

29.5 mL in 1 BOTTLE, DROPPER (63083-9219-1)
Marketing Start Date1985-08-15
NDC Exclude FlagN
Sample Package?N

Drug Details


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