FDA.reportPublic FDA data

Viatrexx-F gus

Manufacturer
VIATREXX BIO INCORPORATED | 8046255 Canada Inc | Les Importations Herbasante Inc
Effective date
2019-03-19
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 02:14:25

Label at a glance#

ProductViatrexx-F gus
Active ingredientEchinacea Angustifolia, Goldenseal, Lycopodium Clavatum Spore, Selenium, Sus Scrofa Thymus, Bos Taurus Thymus, Zinc, Berberis Vulgaris Root Bark, Armoracia Rusticana Whole, Iron, Iridium, Handroanthus Impetiginosus Whole, Lomatium Dissectum Root, Myrrh, Phosphoric Acid, Propolis Wax, Anemone Pulsatilla
Label structure8 sections

Indications and uses

nutritional support for fungal, mold, bacteria challenges 

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Acidum phosphoricum (12X), berberis 3X, Cochlearia armor 3X, Echinacea (3X), ferrum 12X, Hydrastis (3X), iridium 12X, Lapacho 3X, Lomatium 3X, Lycopodium (12X), Myrrh 3X, Propolis 3X, Pulsatilla 12X, Selenium 12X, Thymus (6X), Zinc (12X). 

Description

DESCRIPTION SECTION

Viatrexx-F gus is a homeopathic product composed of physiological (low dose and low low dose) natural micro nutrients. These micro particles are designed to nourish the system.

Uses

INDICATIONS & USAGE SECTION

nutritional support for fungal, mold, bacteria challenges 

Dosage

DOSAGE & ADMINISTRATION SECTION

1-3 spray(s); 1-3 time(s) per day or as recommended by your health care practitioner.

Warnings

WARNINGS SECTION

Stop use and ask a health care practitioner if symptoms persist for more than 5 days or worsen. If pregnant or breastfeeding, ask a health care practitioner before use.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

20% Alcohol and 80% Water.

Product availability

SPL UNCLASSIFIED SECTION

Product may be acquired in 0.5, 30 ,50, 100, 250, 500, 1,000 mL bottles.

References upon request

To report SUSPECTED ADVERSE REACTIONS, contact the FDA at 1-800-FDA-1088 or www.fda.gov/medwatch

Distributed by
Viatrexx Bio Incorporated
Newark, DE, USA, 19713

Manufactured by
8046255 Canada Inc
Beloeil, Qc, J3G 6S3

Date of last revision March 2019

For Questions and comments
Info@Viatrexx.com
www.Viatrexx.com

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC: 63776-175-11
Item: VPC0195

Viatrexx Bio Incorporated

Viatrexx-Fgus 
0.5 mL ampule 
For Oral and Topical Use  

Expiry date:                          Lot #:

Manufactured for: 
Viatrexx Bio Incorporated  Newark, DE, USA, 19713 
www.Viatrexx.com 

Ingredients, homeopathic 

See insert or www.viatrexx.com 

Inactives: Alcohol 20%, Water 80%

NDC: 63776-175-14
Item: VPC0195

Viatrexx Bio Incorporated

Viatrexx-F gus   30 mL spray bottle 
For Oral and Topical Use  

Expiry date:                          Lot #:

Manufactured for: 
Viatrexx Bio Incorporated  Newark, DE, USA, 19713 
www.Viatrexx.com 
Ingredients, homeopathic 

See insert or www.viatrexx.com 

Inactives: Alcohol 20%, Water 80%

fgusfgusNDC: 63776-175-15
Item: VPC07195

Viatrexx Bio Incorporated

Viatrexx-F gus  
50 mL spray bottle 
For Oral and Topical Use  

Expiry date:                          Lot #:

Manufactured for: 
Viatrexx Bio Incorporated  Newark, DE, USA, 19713 
www.Viatrexx.com 
Ingredients, homeopathic 

See insert or www.viatrexx.com 

Inactives: Alcohol 20%, Water 80%

NDC: 63776-175-16
Item: VPC0195

Viatrexx Bio Incorporated

Viatrexx-Fgus  
100 mL bottle 
For Oral and Topical Use  

Expiry date:                          Lot #:

Manufactured for: 
Viatrexx Bio Incorporated  Newark, DE, USA, 19713 
www.Viatrexx.com 
Ingredients, homeopathic 

See insert or www.viatrexx.com 

Inactives: Alcohol 20%, Water 80%

NDC: 63776-175-17
Item: VPC0195

Viatrexx Bio Incorporated

Viatrexx-Fgus   
250 mL bottle 
For Oral and Topical Use  

Expiry date:                          Lot #:

Manufactured for: 
Viatrexx Bio Incorporated  Newark, DE, USA, 19713 
www.Viatrexx.com 
Ingredients, homeopathic 

See insert or www.viatrexx.com 

Inactives: Alcohol 20%, Water 80%

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
86fffa7b-d382-4771-a253-25cccb64b590Product name320251124
910c1bd7-67d1-44c7-ad4f-9445f827edccProduct name120230808
0306390c-dd77-4363-afe0-63c58088b2a1Product name120220120
503ea967-4b9c-48cf-9e87-c7975295849dProduct name220220120
3c386306-c48a-413e-bb69-70cb268496f3Product name120210727
7792dadb-52b6-46b6-8fdf-80b1171065b5Product name120180810

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
63776-175-112022-07-29C16284748780-1e4f33bdf-a60d-d8a0-e053-dadaa90a6e4eF gus
63776-175-142022-07-29C16284748780-1e4f33bdf-a60d-d8a0-e053-dadaa90a6e4eF gus
63776-175-152022-07-29C16284748780-1e4f33bdf-a60d-d8a0-e053-dadaa90a6e4eF gus
63776-175-162022-07-29C16284748780-1e4f33bdf-a60d-d8a0-e053-dadaa90a6e4eF gus
63776-175-172022-07-29C16284748780-1e4f33bdf-a60d-d8a0-e053-dadaa90a6e4eF gus
63776-175-182022-07-29C16284748780-1e4f33bdf-a60d-d8a0-e053-dadaa90a6e4eF gus
63776-175-192022-07-29C16284748780-1e4f33bdf-a60d-d8a0-e053-dadaa90a6e4eF gus

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
63776-175-11Viatrexx-F gus0.5 mL in 1 AMPULESPRAY0.51
63776-175-14Viatrexx-F gus30 mL in 1 BOTTLESPRAY301
63776-175-15Viatrexx-F gus50 mL in 1 BOTTLESPRAY501
63776-175-16Viatrexx-F gus100 mL in 1 BOTTLESPRAY1001
63776-175-17Viatrexx-F gus250 mL in 1 BOTTLESPRAY2501
63776-175-18Viatrexx-F gus500 mL in 1 BOTTLESPRAY5001
63776-175-19Viatrexx-F gus1000 mL in 1 BOTTLESPRAY10001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
63776-175VIATREXX-F GUS (BERBERIS, COCHLEREARIA ARMOR, ECHINACEA, FERRUM, HYDRASTIS, IRIDIUM, LAPACHO, LOMATIUM, LYCOPODIUM, MYRRH, PHOSPORICUM ACIDUM, PROPOLIS, PULSATILLA, SELENEIUM, THYMUS, ZINC) SPRAY [VIATREXX BIO INCORPORATED]1Legacy NDC, 7 package rows20210227_03caaf56-536f-42a8-baed-45263431ee46.zip

Products#

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

DailyMed product names page 1 of 1 · 21 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
63776-17563776-175-15, 63776-175-11, 63776-175-16, 63776-175-17, 63776-175-18, 63776-175-19, 63776-175-14

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 19 matching rows.

Name, UNII, Kind table
NameUNIIKind
Echinacea AngustifoliaVB06AV5US8ACTIB
GoldensealZW3Z11D0JVACTIB
Lycopodium Clavatum SporeC88X29Y479ACTIB
SeleniumH6241UJ22BACTIB
Alcohol3K9958V90MIACT
Water059QF0KO0RIACT
Sus Scrofa Thymus7B69B0BD62ACTIB
Bos Taurus Thymus8XEJ88V2T8ACTIB
ZincJ41CSQ7QDSACTIB
Berberis Vulgaris Root Bark1TH8Q20J0UACTIB
Armoracia Rusticana WholeB18639969QACTIB
IronE1UOL152H7ACTIB
Iridium44448S9773ACTIB
Handroanthus Impetiginosus WholeD65QWF3541ACTIB
Lomatium Dissectum Root5329928G5NACTIB
MyrrhJC71GJ1F3LACTIB
Phosphoric AcidE4GA8884NNACTIB
Propolis Wax6Y8XYV2NOFACTIB
Anemone PulsatillaI76KB35JEVACTIB

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
ad72d2aa-e5bf-4c61-a80d-641b2e20189503caaf56-536f-42a8-baed-45263431ee462019-03-19WarningsExact identifier
spl id: ad72d2aa-e5bf-4c61-a80d-641b2e201895
spl set id: 03caaf56-536f-42a8-baed-45263431ee46

Reported adverse events (FAERS/openFDA)#

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