Pulsatilla

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
Pulsatilla
Generic name
ANEMONE PULSATILLA
Manufacturer
Boiron
Product type
HUMAN OTC DRUG
SPL set ID
86a84380-94f4-41f2-e053-2991aa0a870b
SPL ID
f187d890-3908-8614-e053-2a95a90ab91d
Version
2
Effective date
2023-01-05
Source export date
2026-10-30
Source partition
10
Source file
https://download.open.fda.gov/drug/label/drug-label-0010-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-30/3b4c9bc1c064560160661a043b9878894ba805e5e90f4733fb76824b6ba7ac42/drug-label-0010-of-0014.json.zip
Source manifest SHA-256
b11f1f6b476c7417db937215bf14307ef1a0b69465b42b411ad52f42ae36ead3
Import run
20261102T182004Z
Imported at
2026-11-02 19:22:14
Harmonized routes table
Harmonized routes
ORAL

Reported adverse events (FAERS/openFDA)#

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