BP Reg

Active substance: EPINEPHRINE, GARLIC, ALPHA LIPOIC ACID, SUS SCROFA ARTERY, GOLD, SELENICEREUS GRANDIFLORUS STEM, CHOLESTEROL, CORTISONE ACETATE, COUMARIN, FORMALDEHYDE SOLUTION, NITROGLYCERIN, POTASSIUM CHLORATE, LACHESIS MUTA VENOM, PROTEUS VULGARIS, RAUWOLFIA SERPENTINA, STRONTIUM CARBONATE, SULFUR, THYROID, SUS SCROFA VEIN, VERATRUM ALBUM ROOT

LIQUID · EPINEPHRINE 8 [hp_X]/mL, GARLIC 6 [hp_X]/mL, ALPHA LIPOIC ACID 12 [hp_X]/mL, SUS SCROFA ARTERY 8 [hp_X]/mL, GOLD 12 [hp_X]/mL, SELENICEREUS GRANDIFLORUS STEM 12 [hp_X]/mL, CHOLESTEROL 12 [hp_X]/mL, CORTISONE ACETATE 8 [hp_X]/mL, COUMARIN 12 [hp_X]/mL, FORMALDEHYDE SOLUTION 9 [hp_X]/mL, NITROGLYCERIN 12 [hp_X]/mL, POTASSIUM CHLORATE 9 [hp_X]/mL, LACHESIS MUTA VENOM 12 [hp_X]/mL, PROTEUS VULGARIS 16 [hp_X]/mL, RAUWOLFIA SERPENTINA 12 [hp_X]/mL, STRONTIUM CARBONATE 12 [hp_X]/mL, SULFUR 12 [hp_X]/mL, THYROID 8 [hp_X]/mL, SUS SCROFA VEIN 8 [hp_X]/mL, VERATRUM ALBUM ROOT 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

Composition

EPINEPHRINE · 8 [hp_X]/mL
GARLIC · 6 [hp_X]/mL
ALPHA LIPOIC ACID · 12 [hp_X]/mL
SUS SCROFA ARTERY · 8 [hp_X]/mL
GOLD · 12 [hp_X]/mL
SELENICEREUS GRANDIFLORUS STEM · 12 [hp_X]/mL
CHOLESTEROL · 12 [hp_X]/mL
CORTISONE ACETATE · 8 [hp_X]/mL
COUMARIN · 12 [hp_X]/mL
FORMALDEHYDE SOLUTION · 9 [hp_X]/mL
NITROGLYCERIN · 12 [hp_X]/mL
POTASSIUM CHLORATE · 9 [hp_X]/mL
LACHESIS MUTA VENOM · 12 [hp_X]/mL
PROTEUS VULGARIS · 16 [hp_X]/mL
RAUWOLFIA SERPENTINA · 12 [hp_X]/mL
STRONTIUM CARBONATE · 12 [hp_X]/mL
SULFUR · 12 [hp_X]/mL
THYROID · 8 [hp_X]/mL
SUS SCROFA VEIN · 8 [hp_X]/mL
VERATRUM ALBUM ROOT · 12 [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.

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: 43742-2177
Registration status: Active
Dispensing: Over the counter
Route: ORAL

Sources

product · openFDA NDC · 43742-2177 · Verified 2026-10-09 · open in source
registration_status · openFDA NDC · 43742-2177 · Verified 2026-10-09 · open in source
ingredients.0 · openFDA NDC · 43742-2177 · Verified 2026-10-09 · open in source
ingredients.1 · openFDA NDC · 43742-2177 · Verified 2026-10-09 · open in source
ingredients.2 · openFDA NDC · 43742-2177 · Verified 2026-10-09 · open in source
ingredients.3 · openFDA NDC · 43742-2177 · Verified 2026-10-09 · open in source
ingredients.4 · openFDA NDC · 43742-2177 · Verified 2026-10-09 · open in source
ingredients.5 · openFDA NDC · 43742-2177 · Verified 2026-10-09 · open in source
ingredients.6 · openFDA NDC · 43742-2177 · Verified 2026-10-09 · open in source
ingredients.7 · openFDA NDC · 43742-2177 · Verified 2026-10-09 · open in source
ingredients.8 · openFDA NDC · 43742-2177 · Verified 2026-10-09 · open in source
ingredients.9 · openFDA NDC · 43742-2177 · Verified 2026-10-09 · open in source
ingredients.10 · openFDA NDC · 43742-2177 · Verified 2026-10-09 · open in source
ingredients.11 · openFDA NDC · 43742-2177 · Verified 2026-10-09 · open in source
ingredients.12 · openFDA NDC · 43742-2177 · Verified 2026-10-09 · open in source
ingredients.13 · openFDA NDC · 43742-2177 · Verified 2026-10-09 · open in source
ingredients.14 · openFDA NDC · 43742-2177 · Verified 2026-10-09 · open in source
ingredients.15 · openFDA NDC · 43742-2177 · Verified 2026-10-09 · open in source
ingredients.16 · openFDA NDC · 43742-2177 · Verified 2026-10-09 · open in source
ingredients.17 · openFDA NDC · 43742-2177 · Verified 2026-10-09 · open in source
ingredients.18 · openFDA NDC · 43742-2177 · Verified 2026-10-09 · open in source
ingredients.19 · openFDA NDC · 43742-2177 · Verified 2026-10-09 · open in source