Neurobalance Pro

Manufacturer
The Wellness Center for Reseach and Education, Inc. | Apotheca Company
Effective date
2025-06-06
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 02:33:57

Label at a glance#

ProductNeurobalance Pro
Active ingredient.GAMMA.-AMINOBUTYRIC ACID, GLUTAMIC ACID, NOREPINEPHRINE BITARTRATE, ACETYLCHOLINE CHLORIDE, LEVODOPA, SEROTONIN HYDROCHLORIDE, THYROID, EPINEPHRINE, BARIUM CARBONATE, OYSTER SHELL CALCIUM CARBONATE, CRUDE, SEMECARPUS ANACARDIUM JUICE, CORTICOTROPIN, DATURA STRAMONIUM
Label structure9 sections

Dosage and administration

Spray orally once or twice daily, at least 30 minutes before or after eating. Consult a physician for use in children under 12 years of age.

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS:

OTC - ACTIVE INGREDIENT SECTION

GABA (Gamma-Aminobutyric Acid) 6X, 12X, 30X, 3C, L-Glutamic Acid 6X, 12X, 30X, 3C, Norepinephrine (Bitartrate) 6X, 12X, 30X, 3C, 12C, 30C, Acetylcholine Chloride 6X, 12X, 30X, 3C, 12C, 30C, 1M, L-Dopa 6X, 12X, 30X, 3C, 12C, 30C, 1M, Serotonin (Hydrochloride) 6X, 12X, 30X, 3C, 12C, 30C, 1M, Thyroidinum (Suis) 6X, 12X, 30X 12C, Adrenalinum 10X, 5C, 30C, 1M, Baryta Carbonica 6C, 30C, 200C, Calcarea Carbonica 6C, 30C, 200C, Anacardium Orientale 8C, 30C, 200C, Adrenocorticotrophin 14C, 24C, 30C, Stramonium 30C, 1M.

INDICATIONS:

OTC - PURPOSE SECTION

For the temporary relief of loss of memory, metal weakness, senile dementia, forgetfulness, confusion, anxiety, brain fog, children with slow mental and physical development.

WARNINGS:

WARNINGS SECTION

If pregnant or breast-feeding, ask a health professional before use.

Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.

Do not use if tamper evident seal is broken or missing.

Store in a cool, dry place.

KEEP OUT OF REACH OF CHILDREN:

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.

DIRECTIONS:

DOSAGE & ADMINISTRATION SECTION

Spray orally once or twice daily, at least 30 minutes before or after eating. Consult a physician for use in children under 12 years of age.

INDICATIONS:

INDICATIONS & USAGE SECTION

For the temporary relief of loss of memory, metal weakness, senile dementia, forgetfulness, confusion, anxiety, brain fog, children with slow mental and physical development.

INACTIVE INGREDIENTS:

INACTIVE INGREDIENT SECTION

Demineralized Water, 25% Ethanol

QUESTIONS:

OTC - QUESTIONS SECTION

MFD FOR:

The Wellness Center for Research

and Education, Inc.

1237 S. Victoria Ave. Suite 169

Oxnard, CA 93035

PACKAGE DISPLAY LABEL:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC#: 50181-0070-1

Theresa Dale's

NeuroBalance

PRO

Homeopathic

Neurotransmitter

Formula

1 fl. oz. (30 ml)

NeuroBalance PRONeuroBalance PRO

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
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b5b1095b-40cd-8a9e-b111-502545045b07Product name420250325
e190029e-423b-473c-8e04-2ada59b5b711Product name120250314
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fc363c46-397b-4476-ac0f-70e43e8e4592Product name120150324
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FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
50181-0070-12025-06-06C16284748780-1ba0f9c33-2a79-a910-e053-dadaa90a0b85Drug Facts:
50181-0070-12021-01-29C16284748780-1ba0f9c33-2a79-a910-e053-dadaa90a0b85Drug Facts:

Products#

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

DailyMed product names page 1 of 1 · 22 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
50181-007050181-0070-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 15 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
2fd52df2-1126-4033-9c67-0bc6f012ba0aa37237ed-6465-4623-974d-4f9e22d1e8e92025-06-06WarningsExact identifier
spl id: 2fd52df2-1126-4033-9c67-0bc6f012ba0a
spl set id: a37237ed-6465-4623-974d-4f9e22d1e8e9

Reported adverse events (FAERS/openFDA)#

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