NDC 63479-0302

C02 FIBROZOLVE

Apis Mellifica, Aurum Muriaticum Natronatum, Berberis Vulgaris, Bos Taurus Pituitarum Posterium, Calcarea Fluorica, Calcarea Iodata, Conium Maculatum, Fraxinus Americana, Hydrastis Canadensis, Hydrofluoricum Acidum, Lapis Albus, Pancreatinum, Sarcolacticum Acidum, Sepia, Sulphur Iodatum, Thiosinaminum, Thuja Occidentalis, Thyroidinum

C02 FIBROZOLVE is a Sublingual Solution/ Drops in the Human Otc Drug category. It is labeled and distributed by Apex Energetics Inc.. The primary component is Calcium Hexafluorosilicate; Fraxinus Americana Bark; Lactic Acid, L-; Allylthiourea; Thuja Occidentalis Leafy Twig; Goldenseal; Hydrofluoric Acid; Pancrelipase; Sodium Tetrachloroaurate; Thyroid, Unspecified; Calcium Fluoride; Sepia Officinalis Juice; Sulfur Iodide; Bos Taurus Pituitary Gland, Posterior; Calcium Iodide; Berberis Vulgaris Root Bark; Conium Maculatum Flowering Top; Apis Mellifera.

Product ID63479-0302_b9e51df0-a9a4-30c1-e053-2a95a90a181c
NDC63479-0302
Product TypeHuman Otc Drug
Proprietary NameC02 FIBROZOLVE
Generic NameApis Mellifica, Aurum Muriaticum Natronatum, Berberis Vulgaris, Bos Taurus Pituitarum Posterium, Calcarea Fluorica, Calcarea Iodata, Conium Maculatum, Fraxinus Americana, Hydrastis Canadensis, Hydrofluoricum Acidum, Lapis Albus, Pancreatinum, Sarcolacticum Acidum, Sepia, Sulphur Iodatum, Thiosinaminum, Thuja Occidentalis, Thyroidinum
Dosage FormSolution/ Drops
Route of AdministrationSUBLINGUAL
Marketing Start Date1995-02-15
Marketing CategoryUNAPPROVED HOMEOPATHIC /
Labeler NameApex Energetics Inc.
Substance NameCALCIUM HEXAFLUOROSILICATE; FRAXINUS AMERICANA BARK; LACTIC ACID, L-; ALLYLTHIOUREA; THUJA OCCIDENTALIS LEAFY TWIG; GOLDENSEAL; HYDROFLUORIC ACID; PANCRELIPASE; SODIUM TETRACHLOROAURATE; THYROID, UNSPECIFIED; CALCIUM FLUORIDE; SEPIA OFFICINALIS JUICE; SULFUR IODIDE; BOS TAURUS PITUITARY GLAND, POSTERIOR; CALCIUM IODIDE; BERBERIS VULGARIS ROOT BARK; CONIUM MACULATUM FLOWERING TOP; APIS MELLIFERA
Active Ingredient Strength30 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_C]/mL; [hp_X]/mL; [hp_C]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_C]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
NDC Exclude FlagN
Listing Certified Through2022-12-31

Packaging

NDC 63479-0302-1

30 mL in 1 BOTTLE, GLASS (63479-0302-1)
Marketing Start Date1995-02-15
NDC Exclude FlagN
Sample Package?N

Drug Details


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