Aesculus

openFDA label record#

This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.

Verified complete openFDA source JSON (canonical bytes are SHA-256 checked before publication)

Brand name
Aesculus
Generic name
POTENTILLA ANSERINA, AESCULUS HIPPOCASTANUM, USTILAGO MAIDIS, SECALE CORNUTUM, RUTA GRAVEOLENS
Manufacturer
Marco Pharma International LLC.
Product type
HUMAN OTC DRUG
SPL set ID
99365ce6-f7d1-483b-952b-2ef6a17d39ab
SPL ID
483bfb8e-a23c-8c1c-e063-6294a90abcb1
Version
7
Effective date
2026-01-12
Source export date
2026-11-06
Source partition
3
Source file
https://download.open.fda.gov/drug/label/drug-label-0003-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-11-06/97001096994db9ca8cee114e6c3bb5298d3c573158ffc1ab8692d82e76a3eb40/drug-label-0003-of-0014.json.zip
Source manifest SHA-256
4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
Import run
20261108T063105Z
Imported at
2026-11-08 06:56:00
Harmonized routes table
Harmonized routes
ORAL

Warnings cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Warnings sections page 1 of 1 · 1 matching rows.

warnings

Warnings If pregnant or breast-feeding, consult a health professional before use.

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.