Female Vitality T010
Active substance: BLACK COHOSH, FUCUS VESICULOSUS, SUS SCROFA OVARY, SUS SCROFA PITUITARY GLAND, SUS SCROFA THYROID, GRAPHITE, LACHESIS MUTA VENOM, SODIUM CHLORIDE, ANEMONE PRATENSIS, SEPIA OFFICINALIS JUICE
LIQUID · BLACK COHOSH 3 [hp_X]/mL, FUCUS VESICULOSUS 3 [hp_X]/mL, SUS SCROFA OVARY 6 [hp_X]/mL, SUS SCROFA PITUITARY GLAND 6 [hp_X]/mL, SUS SCROFA THYROID 6 [hp_X]/mL, GRAPHITE 12 [hp_X]/mL, LACHESIS MUTA VENOM 12 [hp_X]/mL, SODIUM CHLORIDE 12 [hp_X]/mL, ANEMONE PRATENSIS 12 [hp_X]/mL, SEPIA OFFICINALIS JUICE 12 [hp_X]/mL
United StatesActive
Marketing holder: Guangzhou Renuma Medical Systems Co., Ltd
Verified 2026-10-09 · openFDA NDC
- Source: openFDA NDC
- Countries with the substance registered: 1
Composition
- BLACK COHOSH · 3 [hp_X]/mL
- FUCUS VESICULOSUS · 3 [hp_X]/mL
- SUS SCROFA OVARY · 6 [hp_X]/mL
- SUS SCROFA PITUITARY GLAND · 6 [hp_X]/mL
- SUS SCROFA THYROID · 6 [hp_X]/mL
- GRAPHITE · 12 [hp_X]/mL
- LACHESIS MUTA VENOM · 12 [hp_X]/mL
- SODIUM CHLORIDE · 12 [hp_X]/mL
- ANEMONE PRATENSIS · 12 [hp_X]/mL
- SEPIA OFFICINALIS JUICE · 12 [hp_X]/mL
Registration
- Registration number
- 71742-0004
- Registration status
- Active
- Dispensing
- Over the counter
- Route
- ORAL
Sources
- product · openFDA NDC · 71742-0004 · Verified 2026-10-09 · open in source
- registration_status · openFDA NDC · 71742-0004 · Verified 2026-10-09 · open in source
- ingredients.0 · openFDA NDC · 71742-0004 · Verified 2026-10-09 · open in source
- ingredients.1 · openFDA NDC · 71742-0004 · Verified 2026-10-09 · open in source
- ingredients.2 · openFDA NDC · 71742-0004 · Verified 2026-10-09 · open in source
- ingredients.3 · openFDA NDC · 71742-0004 · Verified 2026-10-09 · open in source
- ingredients.4 · openFDA NDC · 71742-0004 · Verified 2026-10-09 · open in source
- ingredients.5 · openFDA NDC · 71742-0004 · Verified 2026-10-09 · open in source
- ingredients.6 · openFDA NDC · 71742-0004 · Verified 2026-10-09 · open in source
- ingredients.7 · openFDA NDC · 71742-0004 · Verified 2026-10-09 · open in source
- ingredients.8 · openFDA NDC · 71742-0004 · Verified 2026-10-09 · open in source
- ingredients.9 · openFDA NDC · 71742-0004 · Verified 2026-10-09 · open in source