GUNA ARTHRO RELIEF

Product NDC

17089-463

11-digit product format

170890463

Labeler code

17089

Product ID

17089-463_b258aa33-c259-1343-e053-2a95a90af0c0

Type

HUMAN OTC DRUG

Nonproprietary name

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 -

Dosage form

SOLUTION/ DROPS

Route

ORAL

Labeler

Guna spa

Marketing category

UNAPPROVED HOMEOPATHIC

Marketing start

2020-09-24

Substance

.ALPHA.-KETOGLUTARIC ACID; .ALPHA.-LIPOIC ACID; ASCORBIC ACID; BARIUM OXALOSUCCINATE; BLACK COHOSH; BRYONIA ALBA ROOT; CHLORINE; COLCHICUM AUTUMNALE BULB; NADIDE; OYSTER SHELL CALCIUM CARBONATE, CRUDE; SODIUM DIETHYL OXALACETATE; SODIUM SULFATE; SOLANUM DULCAMARA FLOWER; SULFUR; SUS SCROFA ADRENAL GLAND; SUS SCROFA ARTERY; SUS SCROFA CARTILAGE; SUS SCROFA EMBRYO; SUS SCROFA PLACENTA; SUS SCROFA UMBILICAL CORD; SUS SCROFA VEIN; TOXICODENDRON PUBESCENS LEAF

Active strength

3; 8; 3; 6; 6; 6; 6; 6; 3; 4; 3; 8; 6; 4; 6; 6; 6; 6; 6; 6; 6; 6 [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

Pharmacologic classes

Ascorbic Acid [CS], Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Osmotic Activity [MoA], Osmotic Laxative [EPC], Vitamin C [EPC]

NDC exclude flag

No

Listing certified through

2026-12-31

Current FDA listing

Yes