FDA.reportPublic FDA data

Neuro

Manufacturer
VIATREXX BIO INCORPORATED | Les Importations Herbasante Inc
Effective date
2022-11-30
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-06-01 02:18:42

Label at a glance#

ProductNeuro
Active ingredientDOPAMINE, FERROUS ARSENATE, ABRUS PRECATORIUS SEED, JUNIPERUS SABINA LEAF, LEVODOPA, MELATONIN, RUBIA TINCTORUM WHOLE, SEROTONIN, TAURINE, ANTIARIS TOXICARIA RESIN
Label structure10 sections

Indications and uses

For the support & balancing of the sleep & behavior neurological pathways

Storage and handling

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

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Dopamine 6X 200K, Ferrum Arsenicicum 30K, Jequirity 30K, Juniper Sabina 30K, L-Dopa 6X 200K, Melatonin 6X 200K, Rubia  3X, Serotonin 6X 200K, Taurine 6X 200K, Upas Antiaris 30K,

Purpose:

OTC - PURPOSE SECTION

DopamineNeurological support
Ferrum ArsenicicumEnergy support
JequirityDrainage
Juniper SabinaDrainage
L-DopaNeurological support
MelatoninNeurological support
RubiaImmune support
SerotoninNeurological support
TaurineDrainage
Upas AntiarisDrainage

Uses

INDICATIONS & USAGE SECTION

For the support & balancing of the sleep & behavior neurological pathways

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.

 

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep this and all medicines out of reach of children.

Other Ingredients

INACTIVE INGREDIENT SECTION

Alcohol and Water

Other Information

STORAGE AND HANDLING SECTION

Normal storage use.

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

Questions

OTC - QUESTIONS SECTION

info@viatrexx.com

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

ITEM: VPC0460

NDC 63776-375-15

Homeopathic remedy

Neuro

• For the support & balancing of the sleep & behavior neurological pathways

Oral spray
50ml 1.7 oz

Viatrexx™ Bio Incorporated

Manufactured by Viatrexx
www.viatrexx.com
Newark, DE 19713

carton
carton

Neuro

50 mL
1.7 oz

Viatrexx™ Bio Incorporated

ITEM: VPC0460
NDC: 63776-375-15

INDICATIONS:
For the support & balancing of the sleep & behavior neurological pathways

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

Mfg. for
Viatrexx Bio Incorporated.
www.viatrexx.com
Newark, DE 19713

label
label

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
5ce6fab2-d006-4589-8ba0-02cee499cc60Product name220260128
ebf3b793-6fcd-797b-9d2e-c3faf6d29442Product name520251106
162160fe-5ea6-4f9d-aa38-c4b780c57046Product name120250515
0e5ae331-9620-4d1f-8061-7c437c7f1c42Product name120250312
028fdaca-77da-0dfe-e445-7dfc440fc97eProduct name420250224
de702a02-e9c0-4daf-9101-e44f2c0d4e66Product name120220609
681917df-580c-4199-896d-b739fbb25ed3Product name120190412
6aba2aa6-bc33-4b0c-a81c-06f5fb4cc762Product name220180613
1fa100ae-9ab3-4df0-afe7-33ab01fd4a41Product name120150313
88839c8d-b65b-4a50-997b-4c74539855ffProduct name120150313
b2a69ae1-a082-5ec0-42b6-e3c38800f173Product name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
63776-375-152024-01-30C16284748780-11030e365-404f-111a-e063-dadaa90a10e2Neuro

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
63776-375-15Neuro50 mL in 1 BOTTLE, SPRAYSPRAY504
63776-375-15Neuro1 in 1 BOXSPRAY14

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
63776-375NEURO (INGREDIENTS) SPRAY [VIATREXX BIO INCORPORATED]4Legacy NDC, 2 package rows20221202_310ac221-b74e-49ce-8694-28565f5cc302.zip

Products#

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

DailyMed product names page 1 of 1 · 14 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
63776-37563776-375-15

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 12 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALCOHOL3K9958V90MIACT
WATER059QF0KO0RIACT
DOPAMINEVTD58H1Z2XACTIB
FERROUS ARSENATE129CO35H12ACTIB
ABRUS PRECATORIUS SEED3OM8I6L7CDACTIB
JUNIPERUS SABINA LEAF0R715588D2ACTIB
LEVODOPA46627O600JACTIB
MELATONINJL5DK93RCLACTIB
RUBIA TINCTORUM WHOLEDEF14459OHACTIB
SEROTONIN333DO1RDJYACTIB
TAURINE1EQV5MLY3DACTIB
ANTIARIS TOXICARIA RESINGYD12G07R8ACTIB

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
eeb57e23-467a-a6f0-e053-2995a90a3c75310ac221-b74e-49ce-8694-28565f5cc3022022-11-30WarningsExact identifier
spl id: eeb57e23-467a-a6f0-e053-2995a90a3c75
spl set id: 310ac221-b74e-49ce-8694-28565f5cc302

Reported adverse events (FAERS/openFDA)#

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