MUNDIPUR

Manufacturer
PEKANA Naturheilmittel GmbH
Effective date
2022-12-16
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
full-release
Hydrated at
2026-06-01 02:19:01

Label at a glance#

ProductMUNDIPUR
Active ingredientBryonia Dioica Root, Colchicum autumnale Bulb, Sodium Carbonate, Phytolacca americana Root, Berberis Vulgaris Root Bark, Cynara scolymus Whole, Harpagophytum procumbens Root, Rhododendron Tomentosum Leafy Twig
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Ingredients:
Berberis vulgaris6X
Bryonia cretica4X
Colchicum autumnale12X
Cynara scolymus8X
Harpagophytum procumbens12X
Ledum palustre6X
Natrium carbonicum4X
Phytolacca americana4X

Selected ingredients prepared by spagyric processes.

INACTIVE INGREDIENT SECTION

Contains 20% alcohol by volume.

Indications

INDICATIONS & USAGE SECTION

OTC - PURPOSE SECTION

For relief of occasional minor rheumatic symptoms such as stiffness and joint pain. 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

OTC - ASK DOCTOR 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 - 250 ml Bottle Box

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

MUNDIPUR™

Oral Drops

Homeopathic Medicine

For relief of occasional
minor rheumatic
symptoms such as
stiffness and joint pain

8.5 fl. oz. (250ml)

PEKANA®

PRINCIPAL DISPLAY PANEL - 250 ml Bottle Box
PRINCIPAL DISPLAY PANEL - 250 ml Bottle Box

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
59469-140-50MUNDIPUR250 mL in 1 BOTTLE, GLASSSOLUTION/ DROPS2505
59469-140-50MUNDIPUR1 in 1 BOXSOLUTION/ DROPS15

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
59469-140MUNDIPUR (BRYONIA DIOICA ROOT, COLCHICUM AUTUMNALE BULB, SODIUM CARBONATE, PHYTOLACCA AMERICANA ROOT, BERBERIS VULGARIS ROOT BARK, CYNARA SCOLYMUS WHOLE, HARPAGOPHYTUM PROCUMBENS ROOT, AND LEDUM PALUSTRE TWIG) SOLUTION/ DROPS [PEKANA NATURHEILMITTEL GMBH]5Current NDC, Legacy NDC, 2 package rows20221221_4aeba0c8-0d53-4012-8024-df1e82585cb3.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
59469-14059469-140-50

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
MUNDIPURBRYONIA DIOICA ROOT, COLCHICUM AUTUMNALE BULB, SODIUM CARBONATE, PHYTOLACCA AMERICANA ROOT, BERBERIS VULGARIS ROOT BARK, CYNARA SCOLYMUS WHOLE, HARPAGOPHYTUM PROCUMBENS ROOT, AND LEDUM PALUSTRE TWIGPEKANA Naturheilmittel GmbH4aeba0c8-0d53-4012-8024-df1e82585cb32022-12-16WarningsExact identifier
ndc (package): 59469-140-50
ndc (product): 59469-140
ndc11 (package): 59469014050
spl id: fb347aec-4719-4086-9abd-1c79936b818f
spl set id: 4aeba0c8-0d53-4012-8024-df1e82585cb3

Reported adverse events (FAERS/openFDA)#

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