Viatrexx-Cellulite

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 02:14:24

Label at a glance#

ProductViatrexx-Cellulite
Active ingredientAndrosterone, Artichoke, Adenosine Triphosphate, Basic Fibroblast Growth Factor (Human), Ersofermin, Adenosine Cyclic Phosphate, Levocarnitine, Centella Asiatica, Citric Acid Monohydrate, Cobalt, Estrogens, Esterified, Ferrous Fumarate, Fumaric Acid, Heptaminol, Hamamelis Virginiana Bark, Hyaluronidase, Interleukin-3, Potassium Aspartate, Lactic Acid, Bos Taurus Lymph Vessel, Sus Scrofa Lymph Vessel, Melilotus Officinalis Whole, Manganese, Sodium Diethyl Oxalacetate, Sodium Pyruvate, Quinhydrone, Succinic Acid, Bos Taurus Vein, Sus Scrofa Vein, Vitamin A, Zinc
Label structure10 sections

Indications and uses

Cellulite drainage & tonification, metabolism and lipid balance, hormonal support, circulatory support and regeneration. 

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Androsterone (30K), Artichoke (30K), ATP (30K), bFGF (6X, 200K), cAMP (30K), L-Carnitine (30K), Centella asiatica (6X, 30K), Citric Acid (30K), Cobalt (30K), Estrogen (200K), Ferrum fumaricum (30K), Fumaric acid (30K), Ginkgo (30K), Hamamelis (30K), Hyaluronidase (4X, 30K), IL-3 (8X, 200K), Kalium asparticum (30K), Lactic acid (30K), Lymphatic vessel (8X, 200K), Melilotus (30K), Mn (30K), Natrum oxalaceticum (30K), Natrum pyruvicum (30K), Quinhydrone (30K), Succinic acid (30K), Vein (6X, 200K), Vitamin A (30K), Zinc (30K). 

Purpose

OTC - PURPOSE SECTION

Androsterone
Artichoke
ATP
bFGF
cAMP
L-Carnitine
Centella asiatica
Citric Acid
Cobalt
Estrogen
Ferrum fumaricum
Fumaric acid
Ginkgo
Hamamelis
Hyaluronidase
IL-3
Kalium asparticum
Lactic acid
Lymphatic vessel 
Melilotus
Mn
Natrum oxalaceticum
Natrum pyruvicum
Quinhydrone
Succinic acid
Vein
Vitamin A
Zinc
Hormonal support
Cholesterol balance
Cell respiration
Regeneration
Intra-Cellular support
Metabolic support
Adaptogen
Cell respiration
GI function
Hormonal support
Cell respiration
Cell respiration
Circulation support
Venous support
Regeneration
Immune support
Cell respiration
Cell respiration
Lymphatic support
Drainage
Drainage
Cell respiration
Cell respiration
Krebs cycle support
Cell respiration
Regeneration
Metabolism
Metabolism

Uses

INDICATIONS & USAGE SECTION

Cellulite drainage & tonification, metabolism and lipid balance, hormonal support, circulatory support and regeneration. 

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.

Dosage

DOSAGE & ADMINISTRATION SECTION

1-5 spray(s); 1-3 time(s) per day or as recommended by your health care practitioner.

Product Availability

USE IN SPECIFIC POPULATIONS SECTION

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

Inactive Ingredients

INACTIVE INGREDIENT SECTION

20% Alcohol and 80% Water.

Other Information

OTHER SAFETY INFORMATION

Normal storage use.
Do not use if tamper-evident seal is broken or removed.

References upon request

REFERENCES SECTION

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: 63776-081-11
Item: VPC0076 

Viatrexx Bio Incorporated

Viatrexx-Cellulite  
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: 63776-081-14
Item: VPC0076 

Viatrexx Bio Incorporated

Viatrexx-Cellulite  
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% 

NDC: 63776-081-15
Item: VPC0076 

Viatrexx Bio Incorporated

Viatrexx-Cellulite  
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% 

Label
Label

NDC: 63776-081-16
Item: VPC0076 

Viatrexx Bio Incorporated

Viatrexx-Cellulite  
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: 63776-081-17
Item: VPC0076 

Viatrexx Bio Incorporated

Viatrexx-Cellulite  
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
08c722ec-780f-bb7b-8f14-3d4f7bf0e098Product name220240205
e2f276e5-439f-b432-b5e5-b0cfa993da69Product name320220609
f52be47f-7aa7-46c0-b1fa-50c18dd50206Product name120201029
980b5d64-e8e5-e1c9-b721-75e08f4e00a1Product name220200323
444b3e50-f226-46ef-bfca-2e7035d140cdProduct name120190611
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
0ca1d589-929b-4b33-bc5b-1d84abdafa6aProduct name120150324
fc363c46-397b-4476-ac0f-70e43e8e4592Product name120150324
4585a4fb-0028-3d95-020c-9b1c40bf15e0Product name120140508
597b1cfd-7b31-5048-62be-ca5cd740da2fProduct name120140508
85490a6b-2306-6bf2-c51b-eb63537dc2daProduct name120140508
aaaf3f1f-0ca7-2c75-a463-4dc624538feeProduct name120140508
ec2149b3-5c6d-5344-f757-c86411073075Product name120140508

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
63776-081-11Viatrexx-Cellulite0.5 mL in 1 AMPULESPRAY0.51
63776-081-14Viatrexx-Cellulite30 mL in 1 BOTTLESPRAY301
63776-081-15Viatrexx-Cellulite50 mL in 1 BOTTLESPRAY501
63776-081-16Viatrexx-Cellulite100 mL in 1 BOTTLESPRAY1001
63776-081-17Viatrexx-Cellulite250 mL in 1 BOTTLESPRAY2501
63776-081-18Viatrexx-Cellulite500 mL in 1 BOTTLESPRAY5001
63776-081-19Viatrexx-Cellulite1000 mL in 1 BOTTLESPRAY10001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
63776-081VIATREXX-CELLULITE (ANDROSTERONE, ARTICHOKE, ATP, BFGF, CAMP, L-CARNITINE, CENTELLA ASIATICA, CITRIC ACID, COBALT, ESTROGEN, FERRUM FUMARICUM, FUMARIC ACID, GINKGO, HAMAMELIS, HYALURONIDASE, IL-3, KALIUM ASPARTICUM, LACTIC ACID, LYMPHATIC VESSEL, MELILOTUS, MN, NATRUM OXALACETICUM, NATRUM PYRUVICUM, QUINHYDRONE, SUCCINIC ACID, VEIN, VITAMIN A AND ZINC) SPRAY [VIATREXX BIO INCORPORATED]1Legacy NDC, 7 package rows20210225_e4c2dcfa-46ff-4a26-9610-4042a53e02fc.zip

Products#

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

DailyMed product names page 1 of 2 · 41 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
63776-08163776-081-15, 63776-081-11, 63776-081-16, 63776-081-17, 63776-081-14, 63776-081-18, 63776-081-19

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 33 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
b068f9fb-f2e6-4cbb-9d05-4eff97c95cb3e4c2dcfa-46ff-4a26-9610-4042a53e02fc2019-03-19WarningsExact identifier
spl id: b068f9fb-f2e6-4cbb-9d05-4eff97c95cb3
spl set id: e4c2dcfa-46ff-4a26-9610-4042a53e02fc

Reported adverse events (FAERS/openFDA)#

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