PMS Relief

Active substance: CHASTE TREE FRUIT, BLACK COHOSH, POTASSIUM CARBONATE, LYCOPODIUM CLAVATUM SPORE, SUCROSE, THYROID, BOVINE, SUS SCROFA HYPOTHALAMUS, ARISTOLOCHIA CLEMATITIS ROOT, ESTRONE, GOLD MONOSULFIDE, CANDIDA ALBICANS, ANAMIRTA COCCULUS SEED, CONIUM MACULATUM FLOWERING TOP, CYCLAMEN PURPURASCENS TUBER, MICRURUS CORALLINUS VENOM, CANIS LUPUS FAMILIARIS MILK, LACHESIS MUTA VENOM, MAGNESIUM CARBONATE, PULSATILLA PRATENSIS WHOLE, TIN

LIQUID · CHASTE TREE FRUIT 6 [hp_X]/mL, BLACK COHOSH 6 [hp_X]/mL, POTASSIUM CARBONATE 6 [hp_X]/mL, LYCOPODIUM CLAVATUM SPORE 6 [hp_X]/mL, SUCROSE 6 [hp_X]/mL, THYROID, BOVINE 6 [hp_X]/mL, SUS SCROFA HYPOTHALAMUS 8 [hp_X]/mL, ARISTOLOCHIA CLEMATITIS ROOT 9 [hp_X]/mL, ESTRONE 10 [hp_X]/mL, GOLD MONOSULFIDE 12 [hp_X]/mL, CANDIDA ALBICANS 12 [hp_X]/mL, ANAMIRTA COCCULUS SEED 12 [hp_X]/mL, CONIUM MACULATUM FLOWERING TOP 12 [hp_X]/mL, CYCLAMEN PURPURASCENS TUBER 12 [hp_X]/mL, MICRURUS CORALLINUS VENOM 12 [hp_X]/mL, CANIS LUPUS FAMILIARIS MILK 12 [hp_X]/mL, LACHESIS MUTA VENOM 12 [hp_X]/mL, MAGNESIUM CARBONATE 12 [hp_X]/mL, PULSATILLA PRATENSIS WHOLE 12 [hp_X]/mL, TIN 12 [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

Composition

CHASTE TREE FRUIT · 6 [hp_X]/mL
BLACK COHOSH · 6 [hp_X]/mL
POTASSIUM CARBONATE · 6 [hp_X]/mL
LYCOPODIUM CLAVATUM SPORE · 6 [hp_X]/mL
SUCROSE · 6 [hp_X]/mL
THYROID, BOVINE · 6 [hp_X]/mL
SUS SCROFA HYPOTHALAMUS · 8 [hp_X]/mL
ARISTOLOCHIA CLEMATITIS ROOT · 9 [hp_X]/mL
ESTRONE · 10 [hp_X]/mL
GOLD MONOSULFIDE · 12 [hp_X]/mL
CANDIDA ALBICANS · 12 [hp_X]/mL
ANAMIRTA COCCULUS SEED · 12 [hp_X]/mL
CONIUM MACULATUM FLOWERING TOP · 12 [hp_X]/mL
CYCLAMEN PURPURASCENS TUBER · 12 [hp_X]/mL
MICRURUS CORALLINUS VENOM · 12 [hp_X]/mL
CANIS LUPUS FAMILIARIS MILK · 12 [hp_X]/mL
LACHESIS MUTA VENOM · 12 [hp_X]/mL
MAGNESIUM CARBONATE · 12 [hp_X]/mL
PULSATILLA PRATENSIS WHOLE · 12 [hp_X]/mL
TIN · 12 [hp_X]/mL

Registration

Registration number: 43742-1342
Registration status: Active
Dispensing: Over the counter
Route: ORAL

Sources

product · openFDA NDC · 43742-1342 · Verified 2026-10-09 · open in source
registration_status · openFDA NDC · 43742-1342 · Verified 2026-10-09 · open in source
ingredients.0 · openFDA NDC · 43742-1342 · Verified 2026-10-09 · open in source
ingredients.1 · openFDA NDC · 43742-1342 · Verified 2026-10-09 · open in source
ingredients.2 · openFDA NDC · 43742-1342 · Verified 2026-10-09 · open in source
ingredients.3 · openFDA NDC · 43742-1342 · Verified 2026-10-09 · open in source
ingredients.4 · openFDA NDC · 43742-1342 · Verified 2026-10-09 · open in source
ingredients.5 · openFDA NDC · 43742-1342 · Verified 2026-10-09 · open in source
ingredients.6 · openFDA NDC · 43742-1342 · Verified 2026-10-09 · open in source
ingredients.7 · openFDA NDC · 43742-1342 · Verified 2026-10-09 · open in source
ingredients.8 · openFDA NDC · 43742-1342 · Verified 2026-10-09 · open in source
ingredients.9 · openFDA NDC · 43742-1342 · Verified 2026-10-09 · open in source
ingredients.10 · openFDA NDC · 43742-1342 · Verified 2026-10-09 · open in source
ingredients.11 · openFDA NDC · 43742-1342 · Verified 2026-10-09 · open in source
ingredients.12 · openFDA NDC · 43742-1342 · Verified 2026-10-09 · open in source
ingredients.13 · openFDA NDC · 43742-1342 · Verified 2026-10-09 · open in source
ingredients.14 · openFDA NDC · 43742-1342 · Verified 2026-10-09 · open in source
ingredients.15 · openFDA NDC · 43742-1342 · Verified 2026-10-09 · open in source
ingredients.16 · openFDA NDC · 43742-1342 · Verified 2026-10-09 · open in source
ingredients.17 · openFDA NDC · 43742-1342 · Verified 2026-10-09 · open in source
ingredients.18 · openFDA NDC · 43742-1342 · Verified 2026-10-09 · open in source
ingredients.19 · openFDA NDC · 43742-1342 · Verified 2026-10-09 · open in source