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Emotional Detox and Drainage

Active substance: ACONITUM NAPELLUS WHOLE, EPINEPHRINE, AMBERGRIS, SODIUM TETRACHLOROAURATE, CALCIUM SULFATE ANHYDROUS, BLACK COHOSH, CINCHONA OFFICINALIS BARK, CORTISONE ACETATE, SAFFRON, HERRING SPERM DNA, HYOSCYAMUS NIGER, SUS SCROFA PITUITARY GLAND, SUS SCROFA HYPOTHALAMUS, STRYCHNOS IGNATII SEED, POTASSIUM BROMIDE, LACHESIS MUTA VENOM, PULSATILLA PRATENSIS WHOLE, THYROID, BOVINE, VIOLA ODORATA WHOLE

LIQUID · ACONITUM NAPELLUS WHOLE 6 [hp_X]/mL, EPINEPHRINE 12 [hp_X]/mL, AMBERGRIS 6 [hp_X]/mL, SODIUM TETRACHLOROAURATE 15 [hp_X]/mL, CALCIUM SULFATE ANHYDROUS 6 [hp_X]/mL, BLACK COHOSH 6 [hp_X]/mL, CINCHONA OFFICINALIS BARK 6 [hp_X]/mL, CORTISONE ACETATE 8 [hp_X]/mL, SAFFRON 6 [hp_X]/mL, HERRING SPERM DNA 16 [hp_X]/mL, HYOSCYAMUS NIGER 6 [hp_X]/mL, SUS SCROFA PITUITARY GLAND 8 [hp_X]/mL, SUS SCROFA HYPOTHALAMUS 8 [hp_X]/mL, STRYCHNOS IGNATII SEED 6 [hp_X]/mL, POTASSIUM BROMIDE 6 [hp_X]/mL, LACHESIS MUTA VENOM 12 [hp_X]/mL, PULSATILLA PRATENSIS WHOLE 6 [hp_X]/mL, THYROID, BOVINE 8 [hp_X]/mL, VIOLA ODORATA WHOLE 8 [hp_X]/mL

United StatesActive

Marketing holder: Deseret Biologicals, Inc.

Verified 2026-10-09 · openFDA NDC

Analogues in other countries
Composition
  • ACONITUM NAPELLUS WHOLE · 6 [hp_X]/mL
  • EPINEPHRINE · 12 [hp_X]/mL
  • AMBERGRIS · 6 [hp_X]/mL
  • SODIUM TETRACHLOROAURATE · 15 [hp_X]/mL
  • CALCIUM SULFATE ANHYDROUS · 6 [hp_X]/mL
  • BLACK COHOSH · 6 [hp_X]/mL
  • CINCHONA OFFICINALIS BARK · 6 [hp_X]/mL
  • CORTISONE ACETATE · 8 [hp_X]/mL
  • SAFFRON · 6 [hp_X]/mL
  • HERRING SPERM DNA · 16 [hp_X]/mL
  • HYOSCYAMUS NIGER · 6 [hp_X]/mL
  • SUS SCROFA PITUITARY GLAND · 8 [hp_X]/mL
  • SUS SCROFA HYPOTHALAMUS · 8 [hp_X]/mL
  • STRYCHNOS IGNATII SEED · 6 [hp_X]/mL
  • POTASSIUM BROMIDE · 6 [hp_X]/mL
  • LACHESIS MUTA VENOM · 12 [hp_X]/mL
  • PULSATILLA PRATENSIS WHOLE · 6 [hp_X]/mL
  • THYROID, BOVINE · 8 [hp_X]/mL
  • VIOLA ODORATA WHOLE · 8 [hp_X]/mL
Products containing epinephrine in other countries

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

CountryProducts
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
43742-2542
Registration status
Active
Dispensing
Over the counter
Route
ORAL
Sources
  • product · openFDA NDC · 43742-2542 · Verified 2026-10-09 · open in source
  • registration_status · openFDA NDC · 43742-2542 · Verified 2026-10-09 · open in source
  • ingredients.0 · openFDA NDC · 43742-2542 · Verified 2026-10-09 · open in source
  • ingredients.1 · openFDA NDC · 43742-2542 · Verified 2026-10-09 · open in source
  • ingredients.2 · openFDA NDC · 43742-2542 · Verified 2026-10-09 · open in source
  • ingredients.3 · openFDA NDC · 43742-2542 · Verified 2026-10-09 · open in source
  • ingredients.4 · openFDA NDC · 43742-2542 · Verified 2026-10-09 · open in source
  • ingredients.5 · openFDA NDC · 43742-2542 · Verified 2026-10-09 · open in source
  • ingredients.6 · openFDA NDC · 43742-2542 · Verified 2026-10-09 · open in source
  • ingredients.7 · openFDA NDC · 43742-2542 · Verified 2026-10-09 · open in source
  • ingredients.8 · openFDA NDC · 43742-2542 · Verified 2026-10-09 · open in source
  • ingredients.9 · openFDA NDC · 43742-2542 · Verified 2026-10-09 · open in source
  • ingredients.10 · openFDA NDC · 43742-2542 · Verified 2026-10-09 · open in source
  • ingredients.11 · openFDA NDC · 43742-2542 · Verified 2026-10-09 · open in source
  • ingredients.12 · openFDA NDC · 43742-2542 · Verified 2026-10-09 · open in source
  • ingredients.13 · openFDA NDC · 43742-2542 · Verified 2026-10-09 · open in source
  • ingredients.14 · openFDA NDC · 43742-2542 · Verified 2026-10-09 · open in source
  • ingredients.15 · openFDA NDC · 43742-2542 · Verified 2026-10-09 · open in source
  • ingredients.16 · openFDA NDC · 43742-2542 · Verified 2026-10-09 · open in source
  • ingredients.17 · openFDA NDC · 43742-2542 · Verified 2026-10-09 · open in source
  • ingredients.18 · openFDA NDC · 43742-2542 · Verified 2026-10-09 · open in source