NDC 17089-463

GUNA ARTHRO RELIEF

Arteria Suis - Alpha Ketoglutaricum Acidum - Alpha Lipoicum Acidum - Ascorbicum Acidum - Barium Oxalsuccinicum - Bryonia Alba - Calcarea Carbonica - Cartilago Suis - Chlorinum - Cimicifuga Racemosa - Colchicum Autumnale - Dulcamara - Embryo Suis - Funiculus Umbilicalis Suis - Glandula Suprarenalis Suis - Nadidum - Natrum Oxalaceticum - Natrum Sulphuricum - Placenta Totalis Suis - Rhus Toxicodendron - Sulphur- Vena Suis -

GUNA ARTHRO RELIEF is a Oral Solution/ Drops in the Human Otc Drug category. It is labeled and distributed by Guna Spa. The primary component is Oyster Shell Calcium Carbonate, Crude; Sodium Sulfate; .alpha.-ketoglutaric Acid; .alpha.-lipoic Acid; Sus Scrofa Artery; Ascorbic Acid; Barium Oxalosuccinate; Bryonia Alba Root; Sus Scrofa Cartilage; Chlorine; Black Cohosh; Colchicum Autumnale Bulb; Sus Scrofa Embryo; Solanum Dulcamara Flower; Sus Scrofa Umbilical Cord; Sus Scrofa Adrenal Gland; Nadide; Sodium Diethyl Oxalacetate; Sus Scrofa Placenta; Toxicodendron Pubescens Leaf; Sulfur; Sus Scrofa Vein.

Product ID17089-463_aebb910f-82a6-606d-e053-2a95a90aaad4
NDC17089-463
Product TypeHuman Otc Drug
Proprietary NameGUNA ARTHRO RELIEF
Generic NameArteria Suis - Alpha Ketoglutaricum Acidum - Alpha Lipoicum Acidum - Ascorbicum Acidum - Barium Oxalsuccinicum - Bryonia Alba - Calcarea Carbonica - Cartilago Suis - Chlorinum - Cimicifuga Racemosa - Colchicum Autumnale - Dulcamara - Embryo Suis - Funiculus Umbilicalis Suis - Glandula Suprarenalis Suis - Nadidum - Natrum Oxalaceticum - Natrum Sulphuricum - Placenta Totalis Suis - Rhus Toxicodendron - Sulphur- Vena Suis -
Dosage FormSolution/ Drops
Route of AdministrationORAL
Marketing Start Date2020-09-24
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameGuna spa
Substance NameOYSTER SHELL CALCIUM CARBONATE, CRUDE; SODIUM SULFATE; .ALPHA.-KETOGLUTARIC ACID; .ALPHA.-LIPOIC ACID; SUS SCROFA ARTERY; ASCORBIC ACID; BARIUM OXALOSUCCINATE; BRYONIA ALBA ROOT; SUS SCROFA CARTILAGE; CHLORINE; BLACK COHOSH; COLCHICUM AUTUMNALE BULB; SUS SCROFA EMBRYO; SOLANUM DULCAMARA FLOWER; SUS SCROFA UMBILICAL CORD; SUS SCROFA ADRENAL GLAND; NADIDE; SODIUM DIETHYL OXALACETATE; SUS SCROFA PLACENTA; TOXICODENDRON PUBESCENS LEAF; SULFUR; SUS SCROFA VEIN
Active Ingredient Strength4 [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL
NDC Exclude FlagN
Listing Certified Through2021-12-31

Packaging

NDC 17089-463-18

1 BOTTLE, DROPPER in 1 BOX (17089-463-18) > 30 mL in 1 BOTTLE, DROPPER
Marketing Start Date2020-09-24
NDC Exclude FlagN
Sample Package?N

Drug Details


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