GUNA ARTHRO RELIEF

Active substance: 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

SOLUTION/ DROPS · OYSTER SHELL CALCIUM CARBONATE, CRUDE 4 [hp_X]/30mL, SODIUM SULFATE 8 [hp_X]/30mL, .ALPHA.-KETOGLUTARIC ACID 3 [hp_X]/30mL, .ALPHA.-LIPOIC ACID 8 [hp_X]/30mL, SUS SCROFA ARTERY 6 [hp_X]/30mL, ASCORBIC ACID 3 [hp_X]/30mL, BARIUM OXALOSUCCINATE 6 [hp_X]/30mL, BRYONIA ALBA ROOT 6 [hp_X]/30mL, SUS SCROFA CARTILAGE 6 [hp_X]/30mL, CHLORINE 6 [hp_X]/30mL, BLACK COHOSH 6 [hp_X]/30mL, COLCHICUM AUTUMNALE BULB 6 [hp_X]/30mL, SUS SCROFA EMBRYO 6 [hp_X]/30mL, SOLANUM DULCAMARA FLOWER 6 [hp_X]/30mL, SUS SCROFA UMBILICAL CORD 6 [hp_X]/30mL, SUS SCROFA ADRENAL GLAND 6 [hp_X]/30mL, NADIDE 3 [hp_X]/30mL, SODIUM DIETHYL OXALACETATE 3 [hp_X]/30mL, SUS SCROFA PLACENTA 6 [hp_X]/30mL, TOXICODENDRON PUBESCENS LEAF 6 [hp_X]/30mL, SULFUR 4 [hp_X]/30mL, SUS SCROFA VEIN 6 [hp_X]/30mL

United StatesActive

Marketing holder: Guna spa

Verified 2026-10-09 · openFDA NDC

Source: openFDA NDC
Countries with the substance registered: 1

Composition

OYSTER SHELL CALCIUM CARBONATE, CRUDE · 4 [hp_X]/30mL
SODIUM SULFATE · 8 [hp_X]/30mL
.ALPHA.-KETOGLUTARIC ACID · 3 [hp_X]/30mL
.ALPHA.-LIPOIC ACID · 8 [hp_X]/30mL
SUS SCROFA ARTERY · 6 [hp_X]/30mL
ASCORBIC ACID · 3 [hp_X]/30mL
BARIUM OXALOSUCCINATE · 6 [hp_X]/30mL
BRYONIA ALBA ROOT · 6 [hp_X]/30mL
SUS SCROFA CARTILAGE · 6 [hp_X]/30mL
CHLORINE · 6 [hp_X]/30mL
BLACK COHOSH · 6 [hp_X]/30mL
COLCHICUM AUTUMNALE BULB · 6 [hp_X]/30mL
SUS SCROFA EMBRYO · 6 [hp_X]/30mL
SOLANUM DULCAMARA FLOWER · 6 [hp_X]/30mL
SUS SCROFA UMBILICAL CORD · 6 [hp_X]/30mL
SUS SCROFA ADRENAL GLAND · 6 [hp_X]/30mL
NADIDE · 3 [hp_X]/30mL
SODIUM DIETHYL OXALACETATE · 3 [hp_X]/30mL
SUS SCROFA PLACENTA · 6 [hp_X]/30mL
TOXICODENDRON PUBESCENS LEAF · 6 [hp_X]/30mL
SULFUR · 4 [hp_X]/30mL
SUS SCROFA VEIN · 6 [hp_X]/30mL

Registration

Registration number: 17089-463
Registration status: Active
Dispensing: Over the counter
Route: ORAL

Sources

product · openFDA NDC · 17089-463 · Verified 2026-10-09 · open in source
registration_status · openFDA NDC · 17089-463 · Verified 2026-10-09 · open in source
ingredients.0 · openFDA NDC · 17089-463 · Verified 2026-10-09 · open in source
ingredients.1 · openFDA NDC · 17089-463 · Verified 2026-10-09 · open in source
ingredients.2 · openFDA NDC · 17089-463 · Verified 2026-10-09 · open in source
ingredients.3 · openFDA NDC · 17089-463 · Verified 2026-10-09 · open in source
ingredients.4 · openFDA NDC · 17089-463 · Verified 2026-10-09 · open in source
ingredients.5 · openFDA NDC · 17089-463 · Verified 2026-10-09 · open in source
ingredients.6 · openFDA NDC · 17089-463 · Verified 2026-10-09 · open in source
ingredients.7 · openFDA NDC · 17089-463 · Verified 2026-10-09 · open in source
ingredients.8 · openFDA NDC · 17089-463 · Verified 2026-10-09 · open in source
ingredients.9 · openFDA NDC · 17089-463 · Verified 2026-10-09 · open in source
ingredients.10 · openFDA NDC · 17089-463 · Verified 2026-10-09 · open in source
ingredients.11 · openFDA NDC · 17089-463 · Verified 2026-10-09 · open in source
ingredients.12 · openFDA NDC · 17089-463 · Verified 2026-10-09 · open in source
ingredients.13 · openFDA NDC · 17089-463 · Verified 2026-10-09 · open in source
ingredients.14 · openFDA NDC · 17089-463 · Verified 2026-10-09 · open in source
ingredients.15 · openFDA NDC · 17089-463 · Verified 2026-10-09 · open in source
ingredients.16 · openFDA NDC · 17089-463 · Verified 2026-10-09 · open in source
ingredients.17 · openFDA NDC · 17089-463 · Verified 2026-10-09 · open in source
ingredients.18 · openFDA NDC · 17089-463 · Verified 2026-10-09 · open in source
ingredients.19 · openFDA NDC · 17089-463 · Verified 2026-10-09 · open in source
ingredients.20 · openFDA NDC · 17089-463 · Verified 2026-10-09 · open in source
ingredients.21 · openFDA NDC · 17089-463 · Verified 2026-10-09 · open in source