NDC 63479-0304

C04 ARTHRO MUSCOTOX

Actaea Spicata, Ammonium Benzoicum, Arnica Montana, Bellis Perennis, Berberis Vulgaris, Bryonia, Chelidonium Majus, Chininum Sulphuricum, Dulcamara Lignosa Whole, Echinacea Purpurea, Formica Rufa, Fraxinus Excelsior Leaf, Lacticum Acidum, Ledum Palustre, Pulsatilla Vulgaris, Rhododendron Chrysanthum, Rhus Toxicodendron, Ruta Graveolens, Sarcolacticum Acidum, Symphytum Officinale, Uricum Acidum

C04 ARTHRO MUSCOTOX is a Sublingual Solution/ Drops in the Human Otc Drug category. It is labeled and distributed by Apex Energetics Inc.. The primary component is Solanum Dulcamara Whole; Echinacea Purpurea; Ruta Graveolens Flowering Top; Actaea Spicata Root; Formica Rufa; Fraxinus Excelsior Leaf; Lactic Acid, Dl-; Rhododendron Aureum Leaf; Toxicodendron Pubescens Leaf; Pulsatilla Vulgaris Whole; Rhododendron Tomentosum Leafy Twig; Ammonium Benzoate; Arnica Montana; Berberis Vulgaris Root Bark; Bryonia Alba Root; Lactic Acid, L-; Comfrey Root; Uric Acid; Bellis Perennis; Chelidonium Majus; Quinine Sulfate.

Product ID63479-0304_bc907936-2152-19a8-e053-2a95a90ad97a
NDC63479-0304
Product TypeHuman Otc Drug
Proprietary NameC04 ARTHRO MUSCOTOX
Generic NameActaea Spicata, Ammonium Benzoicum, Arnica Montana, Bellis Perennis, Berberis Vulgaris, Bryonia, Chelidonium Majus, Chininum Sulphuricum, Dulcamara Lignosa Whole, Echinacea Purpurea, Formica Rufa, Fraxinus Excelsior Leaf, Lacticum Acidum, Ledum Palustre, Pulsatilla Vulgaris, Rhododendron Chrysanthum, Rhus Toxicodendron, Ruta Graveolens, Sarcolacticum Acidum, Symphytum Officinale, Uricum Acidum
Dosage FormSolution/ Drops
Route of AdministrationSUBLINGUAL
Marketing Start Date1994-12-15
Marketing CategoryUNAPPROVED HOMEOPATHIC /
Labeler NameApex Energetics Inc.
Substance NameSOLANUM DULCAMARA WHOLE; ECHINACEA PURPUREA; RUTA GRAVEOLENS FLOWERING TOP; ACTAEA SPICATA ROOT; FORMICA RUFA; FRAXINUS EXCELSIOR LEAF; LACTIC ACID, DL-; RHODODENDRON AUREUM LEAF; TOXICODENDRON PUBESCENS LEAF; PULSATILLA VULGARIS WHOLE; RHODODENDRON TOMENTOSUM LEAFY TWIG; AMMONIUM BENZOATE; ARNICA MONTANA; BERBERIS VULGARIS ROOT BARK; BRYONIA ALBA ROOT; LACTIC ACID, L-; COMFREY ROOT; URIC ACID; BELLIS PERENNIS; CHELIDONIUM MAJUS; QUININE SULFATE
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_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; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
NDC Exclude FlagN
Listing Certified Through2022-12-31

Packaging

NDC 63479-0304-1

30 mL in 1 BOTTLE, GLASS (63479-0304-1)
Marketing Start Date1994-12-15
NDC Exclude FlagN
Sample Package?N

Drug Details


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