CARDINORMA

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: CARDINORMA
Generic name: ARNICA MONTANA ROOT, ACTIVATED CHARCOAL, POTASSIUM CARBONATE, LACHESIS MUTA VENOM, NERIUM OLEANDER LEAF, TOBACCO LEAF, PEUMUS BOLDUS LEAF, AND SELENICEREUS GRANDIFLORUS WHOLE
Manufacturer: PEKANA Naturheilmittel GmbH
Product type: HUMAN OTC DRUG
SPL set ID: d84eabc6-c17b-41b9-a450-5ebc0752ca03
SPL ID: ee10404e-1016-4ab0-a62e-fa8c54a39f3b
Version: 2
Effective date: 2023-01-11
Source export date: 2026-11-06
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/2026-11-06/90742968499056f8845d54427ea2950526b02c3f289aedd40679ed8e120a0e89/drug-label-0007-of-0014.json.zip
Source manifest SHA-256: 8dff71fbef1291eb7711013e9a3a06194930757924a8946ae3034107a98d9463
Import run: 20261106T075659Z
Imported at: 2026-11-06 08:43:54

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 · 16 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
brand name		CARDINORMA	openfda.brand_name
generic name		ARNICA MONTANA ROOT, ACTIVATED CHARCOAL, POTASSIUM CARBONATE, LACHESIS MUTA VENOM, NERIUM OLEANDER LEAF, TOBACCO LEAF, PEUMUS BOLDUS LEAF, AND SELENICEREUS GRANDIFLORUS WHOLE	openfda.generic_name
manufacturer name		PEKANA Naturheilmittel GmbH	openfda.manufacturer_name
ndc	package	59469-324-10	openfda.package_ndc
ndc	product	59469-324	openfda.product_ndc
ndc11	package	59469032410	derived:openfda.package_ndc
spl id		ee10404e-1016-4ab0-a62e-fa8c54a39f3b	id
spl set id		d84eabc6-c17b-41b9-a450-5ebc0752ca03	set_id
unii		2P3VWU3H10	openfda.unii
unii		X8H7HS7MRM	openfda.unii
unii		6YR2608RSU	openfda.unii
unii		BQN1B9B9HA	openfda.unii
unii		Q4EWM09M3O	openfda.unii
unii		VSW71SS07I	openfda.unii
unii		7KV510R6H6	openfda.unii
unii		MUE8Y11327	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

Warning If symptoms persist, contact a licensed practitioner. If you have known sensitivity to any of the ingredients, please consult your licensed practitioner before use. If you are pregnant or nursing a baby, seek the advice of a health care professional before use. Keep out of the reach of children. Protect from light and heat.

Reported adverse events (FAERS/openFDA)#

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