Helleborus niger

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: Helleborus niger
Generic name: HELLEBORUS NIGER ROOT
Manufacturer: Washington Homeopathic Products
Product type: HUMAN OTC DRUG
SPL set ID: 0996cbde-0212-ee6b-e063-6394a90a4820
SPL ID: 2cc87829-1807-784b-e063-6394a90ae295
Version: 3
Effective date: 2025-01-28
Source export date: 2026-09-28
Source partition: 11
Source file: https://download.open.fda.gov/drug/label/drug-label-0011-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/aa96b5a2be6b394393acd0090f6948bdf99e0e8e00666f81608929c8fa83db77/drug-label-0011-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 06:16:03

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		Helleborus niger	openfda.brand_name
generic name		HELLEBORUS NIGER ROOT	openfda.generic_name
manufacturer name		Washington Homeopathic Products	openfda.manufacturer_name
ndc	package	71919-818-01	openfda.package_ndc
ndc	product	71919-818	openfda.product_ndc
ndc11	package	71919081801	derived:openfda.package_ndc
spl id		2cc87829-1807-784b-e063-6394a90ae295	id
spl set id		0996cbde-0212-ee6b-e063-6394a90a4820	set_id
unii		608DGJ6815	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

STOP USE AND ASK DOCTOR If symptoms persist or recur, discontinue use. If pregnant or nursing, consult a licensed practitioner before using this product.

Reported adverse events (FAERS/openFDA)#

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