GUNA-ARTHRO

Product NDC

17089-304

11-digit product format

170890304

Labeler code

17089

Product ID

17089-304_ed806a9b-af06-d713-e053-2a95a90a9730

Type

HUMAN OTC DRUG

Nonproprietary name

.ALPHA.-KETOGLUTARIC ACID - ALPHA LIPOIC ACID - ASCORBIC ACID - BARIUM OXALOSUCCINATE - BLACK COHOSH - BRYONIA ALBA ROOT - CALCITONIN HUMAN - CHLORINE - COLCHICUM AUTUMNALE BULB - NADIDE -

Dosage form

SOLUTION/ DROPS

Route

ORAL

Labeler

Guna spa

Marketing category

UNAPPROVED HOMEOPATHIC

Marketing start

2006-05-23

Substance

.ALPHA.-KETOGLUTARIC ACID; .ALPHA.-LIPOIC ACID; ASCORBIC ACID; BARIUM OXALOSUCCINATE; BLACK COHOSH; BRYONIA ALBA ROOT; CALCITONIN HUMAN; CHLORINE; COLCHICUM AUTUMNALE BULB; NADIDE; NERVE GROWTH FACTOR; PRASTERONE; QUINHYDRONE; SODIUM DIETHYL OXALACETATE; SOLANUM DULCAMARA FLOWER; STRONTIUM CARBONATE; SULFUR; SUS SCROFA ADRENAL GLAND; SUS SCROFA ARTERY; SUS SCROFA CARTILAGE; SUS SCROFA CONJUNCTIVA; SUS SCROFA PARATHYROID GLAND; SUS SCROFA PLACENTA; SUS SCROFA UMBILICAL CORD; SUS SCROFA VEIN; TOXICODENDRON PUBESCENS LEAF; VELAFERMIN

Active strength

3; 3; 3; 3; 6; 6; 6; 6; 6; 3; 4; 6; 3; 3; 6; 6; 3; 6; 6; 6; 6; 6; 6; 6; 6; 6; 4 [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_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

Pharmacologic classes

Ascorbic Acid [CS], Depigmenting Activity [PE], Melanin Synthesis Inhibitor [EPC], Melanin Synthesis Inhibitors [MoA], Vitamin C [EPC]

NDC exclude flag

No

Listing certified through

2026-12-31

Current FDA listing

Yes