Spectric
Active substance: AMANITA MUSCARIA FRUITING BODY, ASPARTAME, BUFO BUFO CUTANEOUS GLAND, HUMAN BREAST TUMOR CELL, SUS SCROFA CEREBRUM, ALCOHOL, HELLEBORUS NIGER ROOT, HYDROGEN, HYOSCYAMUS NIGER, POTASSIUM BROMIDE, LEVODOPA, NEON, INDIAN FRANKINCENSE, SUS SCROFA PLACENTA, SEROTONIN HYDROCHLORIDE, DATURA STRAMONIUM, THUJA OCCIDENTALIS LEAFY TWIG
LIQUID · AMANITA MUSCARIA FRUITING BODY 12 [hp_X]/mL, ASPARTAME 6 [hp_X]/mL, BUFO BUFO CUTANEOUS GLAND 12 [hp_X]/mL, HUMAN BREAST TUMOR CELL 30 [hp_X]/mL, SUS SCROFA CEREBRUM 8 [hp_X]/mL, ALCOHOL 6 [hp_X]/mL, HELLEBORUS NIGER ROOT 12 [hp_X]/mL, HYDROGEN 12 [hp_C]/mL, HYOSCYAMUS NIGER 12 [hp_X]/mL, POTASSIUM BROMIDE 6 [hp_X]/mL, LEVODOPA 6 [hp_X]/mL, NEON 16 [hp_C]/mL, INDIAN FRANKINCENSE 12 [hp_X]/mL, SUS SCROFA PLACENTA 8 [hp_X]/mL, SEROTONIN HYDROCHLORIDE 6 [hp_X]/mL, DATURA STRAMONIUM 12 [hp_X]/mL, THUJA OCCIDENTALIS LEAFY TWIG 12 [hp_X]/mL
United StatesActive
Marketing holder: Deseret Biologicals, Inc
Verified 2026-10-09 · openFDA NDC
Analogues in other countries- Source: openFDA NDC
- Countries with the substance registered: 2
- AMANITA MUSCARIA FRUITING BODY · 12 [hp_X]/mL
- ASPARTAME · 6 [hp_X]/mL
- BUFO BUFO CUTANEOUS GLAND · 12 [hp_X]/mL
- HUMAN BREAST TUMOR CELL · 30 [hp_X]/mL
- SUS SCROFA CEREBRUM · 8 [hp_X]/mL
- ALCOHOL · 6 [hp_X]/mL
- HELLEBORUS NIGER ROOT · 12 [hp_X]/mL
- HYDROGEN · 12 [hp_C]/mL
- HYOSCYAMUS NIGER · 12 [hp_X]/mL
- POTASSIUM BROMIDE · 6 [hp_X]/mL
- LEVODOPA · 6 [hp_X]/mL
- NEON · 16 [hp_C]/mL
- INDIAN FRANKINCENSE · 12 [hp_X]/mL
- SUS SCROFA PLACENTA · 8 [hp_X]/mL
- SEROTONIN HYDROCHLORIDE · 6 [hp_X]/mL
- DATURA STRAMONIUM · 12 [hp_X]/mL
- THUJA OCCIDENTALIS LEAFY TWIG · 12 [hp_X]/mL
Showing products with this active substance, combinations included; the full composition is shown for each product.
| Country | Products |
|---|---|
| RU 1 |
|
Control by country
- Russiaprescription only
Source: GRLS (Russian state register) · record 01a120c5-7fb3-7f1c-8b8d-e0142a23c7ff;count=1 · valid from 2026-10-09 · verified 2026-10-09
- Registration number
- 43742-2191
- Registration status
- Active
- Dispensing
- Over the counter
- Route
- ORAL
- product · openFDA NDC · 43742-2191 · Verified 2026-10-09 · open in source
- registration_status · openFDA NDC · 43742-2191 · Verified 2026-10-09 · open in source
- ingredients.0 · openFDA NDC · 43742-2191 · Verified 2026-10-09 · open in source
- ingredients.1 · openFDA NDC · 43742-2191 · Verified 2026-10-09 · open in source
- ingredients.2 · openFDA NDC · 43742-2191 · Verified 2026-10-09 · open in source
- ingredients.3 · openFDA NDC · 43742-2191 · Verified 2026-10-09 · open in source
- ingredients.4 · openFDA NDC · 43742-2191 · Verified 2026-10-09 · open in source
- ingredients.5 · openFDA NDC · 43742-2191 · Verified 2026-10-09 · open in source
- ingredients.6 · openFDA NDC · 43742-2191 · Verified 2026-10-09 · open in source
- ingredients.7 · openFDA NDC · 43742-2191 · Verified 2026-10-09 · open in source
- ingredients.8 · openFDA NDC · 43742-2191 · Verified 2026-10-09 · open in source
- ingredients.9 · openFDA NDC · 43742-2191 · Verified 2026-10-09 · open in source
- ingredients.10 · openFDA NDC · 43742-2191 · Verified 2026-10-09 · open in source
- ingredients.11 · openFDA NDC · 43742-2191 · Verified 2026-10-09 · open in source
- ingredients.12 · openFDA NDC · 43742-2191 · Verified 2026-10-09 · open in source
- ingredients.13 · openFDA NDC · 43742-2191 · Verified 2026-10-09 · open in source
- ingredients.14 · openFDA NDC · 43742-2191 · Verified 2026-10-09 · open in source
- ingredients.15 · openFDA NDC · 43742-2191 · Verified 2026-10-09 · open in source
- ingredients.16 · openFDA NDC · 43742-2191 · Verified 2026-10-09 · open in source