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: PULSATILLA (PRATENSIS)
Manufacturer: Energique, Inc.
Product type: HUMAN OTC DRUG
SPL set ID: 664377e7-2d2f-4a54-bfff-21ff48f7b4ee
SPL ID: e648ebdd-a77d-43b2-ba31-e2dd2d80338c
Version: 4
Effective date: 2024-10-29
Source export date: 2026-09-28
Source partition: 9
Source file: https://download.open.fda.gov/drug/label/drug-label-0009-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/6784607726c827491ceaeab30d843632e0660ee8008c535197be5ed9e1e52201/drug-label-0009-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 06:04:08

Harmonized routes table
Harmonized routes
ORAL

Harmonized identifier links#

Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.

Harmonized identifiers page 1 of 1 · 9 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
brand name		Pulsatilla	openfda.brand_name
generic name		PULSATILLA (PRATENSIS)	openfda.generic_name
manufacturer name		Energique, Inc.	openfda.manufacturer_name
ndc	package	44911-0498-1	openfda.package_ndc
ndc	product	44911-0498	openfda.product_ndc
ndc11	package	44911049801	derived:openfda.package_ndc
spl id		e648ebdd-a77d-43b2-ba31-e2dd2d80338c	id
spl set id		664377e7-2d2f-4a54-bfff-21ff48f7b4ee	set_id
unii		8E272251DI	openfda.unii

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 breastfeeding, ask a health professional before use. Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away. Do not use if tamper evident seal is broken or missing. Store in a cool, dry place.

Reported adverse events (FAERS/openFDA)#

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