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PTS/Stress Remedy

Active substance: DIBASIC POTASSIUM PHOSPHATE, AMBERGRIS, COCOA, PHOSPHORIC ACID, ARNICA MONTANA, OYSTER SHELL CALCIUM CARBONATE, CRUDE, SUS SCROFA CEREBRUM, SUS SCROFA ADRENAL GLAND, LITHIUM CARBONATE, ACONITUM NAPELLUS, ARGEMONE MEXICANA, ARSENIC TRIOXIDE, CICUTA VIROSA ROOT, HYOSCYAMUS NIGER, STRYCHNOS IGNATII SEED, LILIUM LANCIFOLIUM WHOLE FLOWERING, SODIUM CHLORIDE, LYCOSA TARANTULA, DATURA STRAMONIUM, ANDROCTONUS AUSTRALIS VENOM

LIQUID · DIBASIC POTASSIUM PHOSPHATE 3 [hp_X]/mL, AMBERGRIS 6 [hp_X]/mL, COCOA 6 [hp_X]/mL, PHOSPHORIC ACID 6 [hp_X]/mL, ARNICA MONTANA 6 [hp_X]/mL, OYSTER SHELL CALCIUM CARBONATE, CRUDE 8 [hp_X]/mL, SUS SCROFA CEREBRUM 8 [hp_X]/mL, SUS SCROFA ADRENAL GLAND 8 [hp_X]/mL, LITHIUM CARBONATE 8 [hp_X]/mL, ACONITUM NAPELLUS 8 [hp_X]/mL, ARGEMONE MEXICANA 12 [hp_X]/mL, ARSENIC TRIOXIDE 12 [hp_X]/mL, CICUTA VIROSA ROOT 12 [hp_X]/mL, HYOSCYAMUS NIGER 12 [hp_X]/mL, STRYCHNOS IGNATII SEED 12 [hp_X]/mL, LILIUM LANCIFOLIUM WHOLE FLOWERING 12 [hp_X]/mL, SODIUM CHLORIDE 12 [hp_X]/mL, LYCOSA TARANTULA 12 [hp_X]/mL, DATURA STRAMONIUM 12 [hp_X]/mL, ANDROCTONUS AUSTRALIS VENOM 6 [hp_C]/mL

United StatesActive

Marketing holder: Deseret Biologicals, Inc.

Verified 2026-10-09 · openFDA NDC

Composition
  • DIBASIC POTASSIUM PHOSPHATE · 3 [hp_X]/mL
  • AMBERGRIS · 6 [hp_X]/mL
  • COCOA · 6 [hp_X]/mL
  • PHOSPHORIC ACID · 6 [hp_X]/mL
  • ARNICA MONTANA · 6 [hp_X]/mL
  • OYSTER SHELL CALCIUM CARBONATE, CRUDE · 8 [hp_X]/mL
  • SUS SCROFA CEREBRUM · 8 [hp_X]/mL
  • SUS SCROFA ADRENAL GLAND · 8 [hp_X]/mL
  • LITHIUM CARBONATE · 8 [hp_X]/mL
  • ACONITUM NAPELLUS · 8 [hp_X]/mL
  • ARGEMONE MEXICANA · 12 [hp_X]/mL
  • ARSENIC TRIOXIDE · 12 [hp_X]/mL
  • CICUTA VIROSA ROOT · 12 [hp_X]/mL
  • HYOSCYAMUS NIGER · 12 [hp_X]/mL
  • STRYCHNOS IGNATII SEED · 12 [hp_X]/mL
  • LILIUM LANCIFOLIUM WHOLE FLOWERING · 12 [hp_X]/mL
  • SODIUM CHLORIDE · 12 [hp_X]/mL
  • LYCOSA TARANTULA · 12 [hp_X]/mL
  • DATURA STRAMONIUM · 12 [hp_X]/mL
  • ANDROCTONUS AUSTRALIS VENOM · 6 [hp_C]/mL
Registration
Registration number
43742-1322
Registration status
Active
Dispensing
Over the counter
Route
ORAL
Sources
  • product · openFDA NDC · 43742-1322 · Verified 2026-10-09 · open in source
  • registration_status · openFDA NDC · 43742-1322 · Verified 2026-10-09 · open in source
  • ingredients.0 · openFDA NDC · 43742-1322 · Verified 2026-10-09 · open in source
  • ingredients.1 · openFDA NDC · 43742-1322 · Verified 2026-10-09 · open in source
  • ingredients.2 · openFDA NDC · 43742-1322 · Verified 2026-10-09 · open in source
  • ingredients.3 · openFDA NDC · 43742-1322 · Verified 2026-10-09 · open in source
  • ingredients.4 · openFDA NDC · 43742-1322 · Verified 2026-10-09 · open in source
  • ingredients.5 · openFDA NDC · 43742-1322 · Verified 2026-10-09 · open in source
  • ingredients.6 · openFDA NDC · 43742-1322 · Verified 2026-10-09 · open in source
  • ingredients.7 · openFDA NDC · 43742-1322 · Verified 2026-10-09 · open in source
  • ingredients.8 · openFDA NDC · 43742-1322 · Verified 2026-10-09 · open in source
  • ingredients.9 · openFDA NDC · 43742-1322 · Verified 2026-10-09 · open in source
  • ingredients.10 · openFDA NDC · 43742-1322 · Verified 2026-10-09 · open in source
  • ingredients.11 · openFDA NDC · 43742-1322 · Verified 2026-10-09 · open in source
  • ingredients.12 · openFDA NDC · 43742-1322 · Verified 2026-10-09 · open in source
  • ingredients.13 · openFDA NDC · 43742-1322 · Verified 2026-10-09 · open in source
  • ingredients.14 · openFDA NDC · 43742-1322 · Verified 2026-10-09 · open in source
  • ingredients.15 · openFDA NDC · 43742-1322 · Verified 2026-10-09 · open in source
  • ingredients.16 · openFDA NDC · 43742-1322 · Verified 2026-10-09 · open in source
  • ingredients.17 · openFDA NDC · 43742-1322 · Verified 2026-10-09 · open in source
  • ingredients.18 · openFDA NDC · 43742-1322 · Verified 2026-10-09 · open in source
  • ingredients.19 · openFDA NDC · 43742-1322 · Verified 2026-10-09 · open in source