GUNA-DIZZY

Active substance: EPINEPHRINE, .ALPHA.-KETOGLUTARIC ACID, AMBERGRIS, SUS SCROFA ARTERY, SUS SCROFA CEREBELLUM, QUININE SALICYLATE, ANAMIRTA COCCULUS SEED, CONIUM MACULATUM FLOWERING TOP, FUMARIC ACID, MALIC ACID, MELATONIN, MINERAL OIL, SUS SCROFA PLACENTA, PTERIDIUM AQUILINUM ROOT, PYRIDOXINE HYDROCHLORIDE, QUINHYDRONE, TOBACCO LEAF, THIAMINE HYDROCHLORIDE

SOLUTION/ DROPS · EPINEPHRINE 6 [hp_X]/30mL, .ALPHA.-KETOGLUTARIC ACID 6 [hp_X]/30mL, AMBERGRIS 6 [hp_X]/30mL, SUS SCROFA ARTERY 6 [hp_X]/30mL, SUS SCROFA CEREBELLUM 6 [hp_X]/30mL, QUININE SALICYLATE 6 [hp_X]/30mL, ANAMIRTA COCCULUS SEED 4 [hp_X]/30mL, CONIUM MACULATUM FLOWERING TOP 3 [hp_X]/30mL, FUMARIC ACID 6 [hp_X]/30mL, MALIC ACID 6 [hp_X]/30mL, MELATONIN 4 [hp_C]/30mL, MINERAL OIL 8 [hp_X]/30mL, SUS SCROFA PLACENTA 6 [hp_X]/30mL, PTERIDIUM AQUILINUM ROOT 8 [hp_X]/30mL, PYRIDOXINE HYDROCHLORIDE 6 [hp_X]/30mL, QUINHYDRONE 6 [hp_X]/30mL, TOBACCO LEAF 6 [hp_X]/30mL, THIAMINE HYDROCHLORIDE 4 [hp_X]/30mL

United StatesActive

Marketing holder: Guna spa

Verified 2026-10-09 · openFDA NDC

Analogues in other countries

Source: openFDA NDC
Countries with the substance registered: 2

Composition

EPINEPHRINE · 6 [hp_X]/30mL
.ALPHA.-KETOGLUTARIC ACID · 6 [hp_X]/30mL
AMBERGRIS · 6 [hp_X]/30mL
SUS SCROFA ARTERY · 6 [hp_X]/30mL
SUS SCROFA CEREBELLUM · 6 [hp_X]/30mL
QUININE SALICYLATE · 6 [hp_X]/30mL
ANAMIRTA COCCULUS SEED · 4 [hp_X]/30mL
CONIUM MACULATUM FLOWERING TOP · 3 [hp_X]/30mL
FUMARIC ACID · 6 [hp_X]/30mL
MALIC ACID · 6 [hp_X]/30mL
MELATONIN · 4 [hp_C]/30mL
MINERAL OIL · 8 [hp_X]/30mL
SUS SCROFA PLACENTA · 6 [hp_X]/30mL
PTERIDIUM AQUILINUM ROOT · 8 [hp_X]/30mL
PYRIDOXINE HYDROCHLORIDE · 6 [hp_X]/30mL
QUINHYDRONE · 6 [hp_X]/30mL
TOBACCO LEAF · 6 [hp_X]/30mL
THIAMINE HYDROCHLORIDE · 4 [hp_X]/30mL

Products containing epinephrine in other countries

Showing products with this active substance, combinations included; the full composition is shown for each product.

Country	Products
EU 2	Eurneffy epinephrine EMEA/H/C/006139 ALK-Abelló A/S Neffy epinephrine EMEA/H/C/005584 Ars Pharmaceuticals Irl Limited

Registration

Registration number: 17089-306
Registration status: Active
Dispensing: Over the counter
Route: ORAL

Sources

product · openFDA NDC · 17089-306 · Verified 2026-10-09 · open in source
registration_status · openFDA NDC · 17089-306 · Verified 2026-10-09 · open in source
ingredients.0 · openFDA NDC · 17089-306 · Verified 2026-10-09 · open in source
ingredients.1 · openFDA NDC · 17089-306 · Verified 2026-10-09 · open in source
ingredients.2 · openFDA NDC · 17089-306 · Verified 2026-10-09 · open in source
ingredients.3 · openFDA NDC · 17089-306 · Verified 2026-10-09 · open in source
ingredients.4 · openFDA NDC · 17089-306 · Verified 2026-10-09 · open in source
ingredients.5 · openFDA NDC · 17089-306 · Verified 2026-10-09 · open in source
ingredients.6 · openFDA NDC · 17089-306 · Verified 2026-10-09 · open in source
ingredients.7 · openFDA NDC · 17089-306 · Verified 2026-10-09 · open in source
ingredients.8 · openFDA NDC · 17089-306 · Verified 2026-10-09 · open in source
ingredients.9 · openFDA NDC · 17089-306 · Verified 2026-10-09 · open in source
ingredients.10 · openFDA NDC · 17089-306 · Verified 2026-10-09 · open in source
ingredients.11 · openFDA NDC · 17089-306 · Verified 2026-10-09 · open in source
ingredients.12 · openFDA NDC · 17089-306 · Verified 2026-10-09 · open in source
ingredients.13 · openFDA NDC · 17089-306 · Verified 2026-10-09 · open in source
ingredients.14 · openFDA NDC · 17089-306 · Verified 2026-10-09 · open in source
ingredients.15 · openFDA NDC · 17089-306 · Verified 2026-10-09 · open in source
ingredients.16 · openFDA NDC · 17089-306 · Verified 2026-10-09 · open in source
ingredients.17 · openFDA NDC · 17089-306 · Verified 2026-10-09 · open in source