CARDINORMA

Manufacturer
PEKANA Naturheilmittel GmbH
Effective date
2023-01-11
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 02:19:37

Label at a glance#

ProductCARDINORMA
Active ingredientARNICA MONTANA ROOT, ACTIVATED CHARCOAL, POTASSIUM CARBONATE, LACHESIS MUTA VENOM, NERIUM OLEANDER LEAF, TOBACCO LEAF, PEUMUS BOLDUS LEAF, SELENICEREUS GRANDIFLORUS WHOLE
Label structure9 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Ingredients:
Arnica montana4X
Carbo vegetabilis8X
Kalium carbonicum4X
Lachesis muta8X
Nerium oleander4X
Nicotiana tabacum6X
Peumus boldus (Boldo)4X
Selenicereus grandiflorus4X

Selected ingredients prepared by spagyric processes.

INACTIVE INGREDIENT SECTION

Contains 19% alcohol by volume.

Indications

INDICATIONS & USAGE SECTION

OTC - PURPOSE SECTION

For occasional tiredness often experienced by the elderly. Application of this homeopathic remedy for the designated usage is exclusively based on homeopathic experience. With severe forms of this disease, a clinically proven therapy is indicated.

Dosage

DOSAGE & ADMINISTRATION SECTION

Unless otherwise prescribed, adults take 15-20 drops, 3 times per day. For pediatric dosages, consult your practitioner.

Warning

WARNINGS SECTION

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.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of the reach of children.

STORAGE AND HANDLING SECTION

Protect from light and heat.

Tamper Evident

SPL UNCLASSIFIED SECTION

Do not use this product if tamper evident strip is broken or removed from base of cap.

OTC - QUESTIONS SECTION

To report adverse events, contact BioResource at 321B Blodgett Street, Cotati, CA 94931

SPL UNCLASSIFIED SECTION

Distributed by:
BioResource Inc.
Cotati, CA 94931

Manufactured by:
PEKANA® GmbH
D-88353 Kisslegg

PRINCIPAL DISPLAY PANEL - 50 ml Bottle Box

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

CARDINORMA™
Oral Drops

Homeopathic Medicine

For occasional
tiredness often
experienced by
the elderly

1.7 FL OZ
(50 ml)

PEKANA®

PRINCIPAL DISPLAY PANEL - 50 ml Bottle Box
PRINCIPAL DISPLAY PANEL - 50 ml Bottle Box

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
59469-324-10CARDINORMA1 in 1 BOXSOLUTION/ DROPS12
59469-324-10CARDINORMA50 mL in 1 BOTTLE, GLASSSOLUTION/ DROPS502

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
59469-324CARDINORMA (ARNICA MONTANA ROOT, ACTIVATED CHARCOAL, POTASSIUM CARBONATE, LACHESIS MUTA VENOM, NERIUM OLEANDER LEAF, TOBACCO LEAF, PEUMUS BOLDUS LEAF, AND SELENICEREUS GRANDIFLORUS WHOLE) SOLUTION/ DROPS [PEKANA NATURHEILMITTEL GMBH]2Current NDC, Legacy NDC, 2 package rows20230113_d84eabc6-c17b-41b9-a450-5ebc0752ca03.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 13 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
59469-32459469-324-10

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 10 matching rows.

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
CARDINORMAARNICA MONTANA ROOT, ACTIVATED CHARCOAL, POTASSIUM CARBONATE, LACHESIS MUTA VENOM, NERIUM OLEANDER LEAF, TOBACCO LEAF, PEUMUS BOLDUS LEAF, AND SELENICEREUS GRANDIFLORUS WHOLEPEKANA Naturheilmittel GmbHd84eabc6-c17b-41b9-a450-5ebc0752ca032023-01-11WarningsExact identifier
ndc (package): 59469-324-10
ndc (product): 59469-324
ndc11 (package): 59469032410
spl id: ee10404e-1016-4ab0-a62e-fa8c54a39f3b
spl set id: d84eabc6-c17b-41b9-a450-5ebc0752ca03

Reported adverse events (FAERS/openFDA)#

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