Ignatia

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: Ignatia
Generic name: IGNATIA AMARA
Manufacturer: Historical Remedies
Product type: HUMAN OTC DRUG
SPL set ID: 2e973fcf-9012-4b90-e063-6394a90afe7d
SPL ID: 2e9733a2-c7b5-2eec-e063-6394a90aa009
Version: 1
Effective date: 2025-02-20
Source export date: 2026-10-27
Source partition: 7
Source file: https://download.open.fda.gov/drug/label/drug-label-0007-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-27/be847f9aea8d80a2cb7e9771acd1143be084664192ecf8f5be8ac1024116f4f0/drug-label-0007-of-0014.json.zip
Source manifest SHA-256: 6be3667a3beefe6c0ead4c723ea963050533a2bc725a8044d58b07d18b258c55
Import run: 20261027T193451Z
Imported at: 2026-10-27 20:13:25

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		Ignatia	openfda.brand_name
generic name		IGNATIA AMARA	openfda.generic_name
manufacturer name		Historical Remedies	openfda.manufacturer_name
ndc	package	57556-014-02	openfda.package_ndc
ndc	product	57556-014	openfda.product_ndc
ndc11	package	57556001402	derived:openfda.package_ndc
spl id		2e9733a2-c7b5-2eec-e063-6394a90aa009	id
spl set id		2e973fcf-9012-4b90-e063-6394a90afe7d	set_id
unii		1NM3M2487K	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 SECTION Warning : Consult a doctor if symptoms persist more than 3 days or worsen. If pregnant or nursing , ask a doctor before use. Keep out of reach of children. Do not use if tamper-evident band is missing or broken.

Reported adverse events (FAERS/openFDA)#

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