HABIFAC

Manufacturer
PEKANA Naturheilmittel GmbH
Effective date
2022-12-15
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
full-release
Hydrated at
2026-06-01 02:18:55

Label at a glance#

ProductHABIFAC
Active ingredientFormic Acid, Nitric Acid, Baptisia tinctoria Root, Graphite, Calcium sulfide, Thuja occidentalis Leafy Twig, Vincetoxicum Hirundinaria Leaf, Glechoma hederacea Flowering Top
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Ingredients:
Acidum formicicum8X
Acidum nitricum6X
Baptisia tinctora5X
Glechoma hederacea4X
Graphites8X
Hepar sulfuris8X
Thuja occidentalis10X
Vincetoxicum hirundinaria8X

Selected ingredients prepared by spagyric processes.

INACTIVE INGREDIENT SECTION

Contains 17% alcohol by volume.

Indications

INDICATIONS & USAGE SECTION

OTC - PURPOSE SECTION

Restorative remedy for minor systemic weakness. 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

HABIFAC™
Oral Drops

Homeopathic Medicine

Restorative remedy
for minor systemic
weakness

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
59469-141-10HABIFAC1 in 1 BOXSOLUTION/ DROPS15
59469-141-10HABIFAC50 mL in 1 BOTTLE, GLASSSOLUTION/ DROPS505

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
59469-141HABIFAC (FORMIC ACID, NITRIC ACID, BAPTISIA TINCTORIA ROOT, GRAPHITE, CALCIUM SULFIDE, THUJA OCCIDENTALIS LEAFY TWIG, CYNANCHUM VINCETOXICUM LEAF, AND GLECHOMA HEDERACEA FLOWERING TOP) SOLUTION/ DROPS [PEKANA NATURHEILMITTEL GMBH]5Current NDC, Legacy NDC, 2 package rows20221217_b5fd91ae-3822-421a-a449-4178111950bc.zip

Products#

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

DailyMed product names page 1 of 1 · 12 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
59469-14159469-141-10

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
HABIFACFORMIC ACID, NITRIC ACID, BAPTISIA TINCTORIA ROOT, GRAPHITE, CALCIUM SULFIDE, THUJA OCCIDENTALIS LEAFY TWIG, CYNANCHUM VINCETOXICUM LEAF, AND GLECHOMA HEDERACEA FLOWERING TOPPEKANA Naturheilmittel GmbHb5fd91ae-3822-421a-a449-4178111950bc2022-12-15WarningsExact identifier
ndc (package): 59469-141-10
ndc (product): 59469-141
ndc11 (package): 59469014110
spl id: 2989c3c6-5187-4615-8c71-31912aa57a10
spl set id: b5fd91ae-3822-421a-a449-4178111950bc

Reported adverse events (FAERS/openFDA)#

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