NDC 17089-304

GUNA-ARTHRO

.alpha.-ketoglutaric Acid - Alpha Lipoic Acid - Ascorbic Acid - Barium Oxalosuccinate - Black Cohosh - Bryonia Alba Root - Calcitonin Human - Chlorine - Colchicum Autumnale Bulb - Nadide -

GUNA-ARTHRO is a Oral Solution/ Drops in the Human Otc Drug category. It is labeled and distributed by Guna Spa. The primary component is .alpha.-ketoglutaric Acid; .alpha.-lipoic Acid; Sus Scrofa Artery; Ascorbic Acid; Barium Oxalosuccinate; Bryonia Alba Root; Calcitonin Human; Sus Scrofa Cartilage; Chlorine; Black Cohosh; Colchicum Autumnale Bulb; Sus Scrofa Conjunctiva; Solanum Dulcamara Flower; Velafermin; Sus Scrofa Umbilical Cord; Sus Scrofa Adrenal Gland; Nadide; Sodium Diethyl Oxalacetate; Nerve Growth Factor; Sus Scrofa Parathyroid Gland; Sus Scrofa Placenta; Quinhydrone; Toxicodendron Pubescens Leaf; Strontium Carbonate; Sulfur; Sus Scrofa Vein; Prasterone.

Product ID17089-304_7df285bd-82b9-8907-e053-2a91aa0ac403
NDC17089-304
Product TypeHuman Otc Drug
Proprietary NameGUNA-ARTHRO
Generic Name.alpha.-ketoglutaric Acid - Alpha Lipoic Acid - Ascorbic Acid - Barium Oxalosuccinate - Black Cohosh - Bryonia Alba Root - Calcitonin Human - Chlorine - Colchicum Autumnale Bulb - Nadide -
Dosage FormSolution/ Drops
Route of AdministrationORAL
Marketing Start Date2006-05-23
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameGuna spa
Substance Name.ALPHA.-KETOGLUTARIC ACID; .ALPHA.-LIPOIC ACID; SUS SCROFA ARTERY; ASCORBIC ACID; BARIUM OXALOSUCCINATE; BRYONIA ALBA ROOT; CALCITONIN HUMAN; SUS SCROFA CARTILAGE; CHLORINE; BLACK COHOSH; COLCHICUM AUTUMNALE BULB; SUS SCROFA CONJUNCTIVA; SOLANUM DULCAMARA FLOWER; VELAFERMIN; SUS SCROFA UMBILICAL CORD; SUS SCROFA ADRENAL GLAND; NADIDE; SODIUM DIETHYL OXALACETATE; NERVE GROWTH FACTOR; SUS SCROFA PARATHYROID GLAND; SUS SCROFA PLACENTA; QUINHYDRONE; TOXICODENDRON PUBESCENS LEAF; STRONTIUM CARBONATE; SULFUR; SUS SCROFA VEIN; PRASTERONE
Active Ingredient Strength3 [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_C]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_C]/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 Through2019-12-31

Packaging

NDC 17089-304-18

1 BOTTLE, DROPPER in 1 BOX (17089-304-18) > 30 mL in 1 BOTTLE, DROPPER
Marketing Start Date2018-12-21
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 17089-304-18 [17089030418]

GUNA-ARTHRO SOLUTION/ DROPS
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-12-21
Inactivation Date2020-01-31
Reactivation Date2020-03-13

Drug Details


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