PTS/Stress Remedy
Active substance: ACONITUM NAPELLUS WHOLE, AMBERGRIS, ARGEMONE MEXICANA, ARNICA MONTANA WHOLE, ARSENIC TRIOXIDE, ANDROCTONUS AUSTRALIS VENOM, COCOA, OYSTER SHELL CALCIUM CARBONATE, CRUDE, SUS SCROFA CEREBRUM, CICUTA VIROSA ROOT, SUS SCROFA ADRENAL GLAND, HYOSCYAMUS NIGER, STRYCHNOS IGNATII SEED, DIBASIC POTASSIUM PHOSPHATE, LILIUM LANCIFOLIUM WHOLE FLOWERING, LITHIUM CARBONATE, SODIUM CHLORIDE, PHOSPHORIC ACID, DATURA STRAMONIUM, LYCOSA TARANTULA
LIQUID · ACONITUM NAPELLUS WHOLE 8 [hp_X]/mL, AMBERGRIS 6 [hp_X]/mL, ARGEMONE MEXICANA 12 [hp_X]/mL, ARNICA MONTANA WHOLE 6 [hp_X]/mL, ARSENIC TRIOXIDE 12 [hp_X]/mL, ANDROCTONUS AUSTRALIS VENOM 12 [hp_X]/mL, COCOA 6 [hp_X]/mL, OYSTER SHELL CALCIUM CARBONATE, CRUDE 8 [hp_X]/mL, SUS SCROFA CEREBRUM 8 [hp_X]/mL, CICUTA VIROSA ROOT 12 [hp_X]/mL, SUS SCROFA ADRENAL GLAND 8 [hp_X]/mL, HYOSCYAMUS NIGER 12 [hp_X]/mL, STRYCHNOS IGNATII SEED 12 [hp_X]/mL, DIBASIC POTASSIUM PHOSPHATE 3 [hp_X]/mL, LILIUM LANCIFOLIUM WHOLE FLOWERING 12 [hp_X]/mL, LITHIUM CARBONATE 8 [hp_X]/mL, SODIUM CHLORIDE 12 [hp_X]/mL, PHOSPHORIC ACID 6 [hp_X]/mL, DATURA STRAMONIUM 12 [hp_X]/mL, LYCOSA TARANTULA 16 [hp_X]/mL
United StatesActive
Marketing holder: Deseret Biologicals, Inc.
Verified 2026-10-09 · openFDA NDC
- Source: openFDA NDC
- Countries with the substance registered: 1
- ACONITUM NAPELLUS WHOLE · 8 [hp_X]/mL
- AMBERGRIS · 6 [hp_X]/mL
- ARGEMONE MEXICANA · 12 [hp_X]/mL
- ARNICA MONTANA WHOLE · 6 [hp_X]/mL
- ARSENIC TRIOXIDE · 12 [hp_X]/mL
- ANDROCTONUS AUSTRALIS VENOM · 12 [hp_X]/mL
- COCOA · 6 [hp_X]/mL
- OYSTER SHELL CALCIUM CARBONATE, CRUDE · 8 [hp_X]/mL
- SUS SCROFA CEREBRUM · 8 [hp_X]/mL
- CICUTA VIROSA ROOT · 12 [hp_X]/mL
- SUS SCROFA ADRENAL GLAND · 8 [hp_X]/mL
- HYOSCYAMUS NIGER · 12 [hp_X]/mL
- STRYCHNOS IGNATII SEED · 12 [hp_X]/mL
- DIBASIC POTASSIUM PHOSPHATE · 3 [hp_X]/mL
- LILIUM LANCIFOLIUM WHOLE FLOWERING · 12 [hp_X]/mL
- LITHIUM CARBONATE · 8 [hp_X]/mL
- SODIUM CHLORIDE · 12 [hp_X]/mL
- PHOSPHORIC ACID · 6 [hp_X]/mL
- DATURA STRAMONIUM · 12 [hp_X]/mL
- LYCOSA TARANTULA · 16 [hp_X]/mL
- Registration number
- 43742-2245
- Registration status
- Active
- Dispensing
- Over the counter
- Route
- ORAL
- product · openFDA NDC · 43742-2245 · Verified 2026-10-09 · open in source
- registration_status · openFDA NDC · 43742-2245 · Verified 2026-10-09 · open in source
- ingredients.0 · openFDA NDC · 43742-2245 · Verified 2026-10-09 · open in source
- ingredients.1 · openFDA NDC · 43742-2245 · Verified 2026-10-09 · open in source
- ingredients.2 · openFDA NDC · 43742-2245 · Verified 2026-10-09 · open in source
- ingredients.3 · openFDA NDC · 43742-2245 · Verified 2026-10-09 · open in source
- ingredients.4 · openFDA NDC · 43742-2245 · Verified 2026-10-09 · open in source
- ingredients.5 · openFDA NDC · 43742-2245 · Verified 2026-10-09 · open in source
- ingredients.6 · openFDA NDC · 43742-2245 · Verified 2026-10-09 · open in source
- ingredients.7 · openFDA NDC · 43742-2245 · Verified 2026-10-09 · open in source
- ingredients.8 · openFDA NDC · 43742-2245 · Verified 2026-10-09 · open in source
- ingredients.9 · openFDA NDC · 43742-2245 · Verified 2026-10-09 · open in source
- ingredients.10 · openFDA NDC · 43742-2245 · Verified 2026-10-09 · open in source
- ingredients.11 · openFDA NDC · 43742-2245 · Verified 2026-10-09 · open in source
- ingredients.12 · openFDA NDC · 43742-2245 · Verified 2026-10-09 · open in source
- ingredients.13 · openFDA NDC · 43742-2245 · Verified 2026-10-09 · open in source
- ingredients.14 · openFDA NDC · 43742-2245 · Verified 2026-10-09 · open in source
- ingredients.15 · openFDA NDC · 43742-2245 · Verified 2026-10-09 · open in source
- ingredients.16 · openFDA NDC · 43742-2245 · Verified 2026-10-09 · open in source
- ingredients.17 · openFDA NDC · 43742-2245 · Verified 2026-10-09 · open in source
- ingredients.18 · openFDA NDC · 43742-2245 · Verified 2026-10-09 · open in source
- ingredients.19 · openFDA NDC · 43742-2245 · Verified 2026-10-09 · open in source