United States · FDA National Drug Code directory
Aesculus
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 60986-1027_483bfb8e-a23c-8c1c-e063-6294a90abcb1
- Product NDC
- 60986-1027
- Form
- LIQUID
- Composition / generic term
- Potentilla Anserina, Aesculus Hippocastanum, Ustilago Maidis, Secale Cornutum, Ruta Graveolens
- Labeler
- Marco Pharma International LLC.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start / end (source format)
- 19920301
- Source listing expiry
- 20271231
Source-listed ingredients
- ARGENTINA ANSERINA FLOWERING TOP — 1 [hp_X]/mL
- HORSE CHESTNUT — 1 [hp_X]/mL
- USTILAGO MAYDIS — 5 [hp_X]/mL
- CLAVICEPS PURPUREA SCLEROTIUM — 4 [hp_X]/mL
- RUTA GRAVEOLENS WHOLE — 3 [hp_X]/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 50 mL in 1 BOTTLE, GLASS (60986-1027-3) · 60986-1027-3
- 100 mL in 1 BOTTLE, GLASS (60986-1027-4) · 60986-1027-4
Source and coverage
Open FDA National Drug Code directory →
Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
Browse United States records →