Neuro-Pro

Manufacturer
Guangzhou Renuma Medical Systems Co., Ltd | Apotheca Company
Effective date
2017-10-18
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 02:08:55

Label at a glance#

ProductNeuro-Pro T007
Active ingredient.GAMMA.-AMINOBUTYRIC ACID, LEVODOPA, NOREPINEPHRINE, SEROTONIN HYDROCHLORIDE, CORTICOTROPIN, ANACARDIUM OCCIDENTALE FRUIT, ARSENIC TRIOXIDE, BARIUM CARBONATE, OYSTER SHELL CALCIUM CARBONATE, CRUDE, TRIBASIC CALCIUM PHOSPHATE, HYOSCYAMUS NIGER, LYCOPODIUM CLAVATUM SPORE, DATURA STRAMONIUM
Label structure9 sections

Dosage and administration

Adults and children 5 to 10 drops orally, 1 to 2 times daily or as otherwise directed by a health care professional. If symptoms persist, consult your health care professional. 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, 12C, 30C, L-Dopa 6X, 12X, 30X, 12C, 30C, Norepinephrine 6X, 12X, 30C, 12C, 30C, Serotonin (Hydrochloride) 6X, 12X, 30X, 12C, 30C, Adrenocorticotrophin 8X, 12X, 30X, 12C, 30C, Anacardium Orientale 30C, Arsenicum Album 30C, Baryta Carbonica 30C, Calcarea Carbonica 30C, Calcarea Phosphorica 30C, Hyoscyamus Niger 30C, Lycopodium Clavatum 30C, Stramonium 30C.

INDICATIONS:

OTC - PURPOSE SECTION

May temporarily relieve symptoms associated with attention disorders.

WARNINGS:

WARNINGS SECTION

If pregnant or breast-feeding, ask a health care 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 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

Adults and children 5 to 10 drops orally, 1 to 2 times daily or as otherwise directed by a health care professional. If symptoms persist, consult your health care professional. Consult a physician for use in children under 12 years of age.

INDICATIONS:

INDICATIONS & USAGE SECTION

May temporarily relieve symptoms associated with attention disorders.

INACTIVE INGREDIENTS:

INACTIVE INGREDIENT SECTION

Demineralized water, Glycerin

QUESTIONS:

OTC - QUESTIONS SECTION

Distributed by:

Guangzhou Renuma Medical

Systems Co., Ltd.

No. 5, 2nd Floor, Ascendas 2nd Street

Sino-Singapore Guangzhou Knowledge City

Guangzhou 510555, China

PACKAGE LABEL DISPLAY:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NEURO-PRO

T007

HOMEOPATHIC

2 fl. oz. (59 ml)

Neuro-Pro T007Neuro-Pro T007

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
5ce6fab2-d006-4589-8ba0-02cee499cc60Product name220260128
2ab36713-99a4-1d04-c42f-907afc73b6f9Product name720260105
ebf3b793-6fcd-797b-9d2e-c3faf6d29442Product name520251106
bee4fa8d-8d82-423a-a0b5-40a89dd13a99Product name120250618
e0d2eb29-08bd-4bba-90d1-c91c68a38767Product name420250516
162160fe-5ea6-4f9d-aa38-c4b780c57046Product name120250515
0e5ae331-9620-4d1f-8061-7c437c7f1c42Product name120250312
30b0ac6e-02aa-0e5c-0d8b-cffdf3a282b2Product name520250304
028fdaca-77da-0dfe-e445-7dfc440fc97eProduct name420250224
7314d8f7-fa99-4dc2-9f68-de2ff142f4b7Product name220250121
63f39a63-5cd1-4016-bd86-2bbb0f6c3139Product name320240506
e5a77e9c-c528-733a-173d-914a234c024bProduct name520240506
334fe8d2-68fb-4331-a576-420e302ec069Product name720240320
209a4db0-2639-413d-9ad3-274ad7be11f7Product name120230912
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de702a02-e9c0-4daf-9101-e44f2c0d4e66Product name120220609
444b3e50-f226-46ef-bfca-2e7035d140cdProduct name120190611
681917df-580c-4199-896d-b739fbb25ed3Product name120190412
e92765c1-be81-432a-b909-1b10777ec378Product name120190208
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
d5e51f11-ad28-caa4-4b49-4143974782adProduct name120150831
0ca1d589-929b-4b33-bc5b-1d84abdafa6aProduct name120150324
fc363c46-397b-4476-ac0f-70e43e8e4592Product name120150324
0441a8f5-3835-497c-aedd-bc78cba56b2aProduct name120150317
1fa100ae-9ab3-4df0-afe7-33ab01fd4a41Product name120150313
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DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
71742-0001-1Neuro-ProT00759 mL in 1 BOTTLE, DROPPERLIQUID591

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
71742-0001NEURO-PRO T007 (GABA, L-DOPA, NOREPINEPHRINE, SEROTONIN, ADRENOCORTICOTROPHIN, ANACARDIUM ORIENTALE, ARSENICUM ALBUM, BARYTA CARBONICA, CALCAREA CARBONICA, CALCAREA PHOSPHORICA, HYOSCYAMUS NIGER, LYCOPODIUM CLAVATUM, STRAMONIUM) LIQUID [GUANGZHOU RENUMA MEDICAL SYSTEMS CO., LTD]1Current NDC, Legacy NDC, 1 package rows20171021_7e02ab0c-9bc2-4ffe-926c-5b388a07f7b2.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
71742-000171742-0001-1

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
Neuro-Pro T007GABA, L-DOPA, NOREPINEPHRINE, SEROTONIN, ADRENOCORTICOTROPHIN, ANACARDIUM ORIENTALE, ARSENICUM ALBUM, BARYTA CARBONICA, CALCAREA CARBONICA, CALCAREA PHOSPHORICA, HYOSCYAMUS NIGER, LYCOPODIUM CLAVATUM, STRAMONIUMGuangzhou Renuma Medical Systems Co., Ltd7e02ab0c-9bc2-4ffe-926c-5b388a07f7b22017-10-18WarningsExact identifier
ndc (package): 71742-0001-1
ndc (product): 71742-0001
ndc11 (package): 71742000101
spl id: 33bf81ec-4693-464f-ab65-61cce5756124
spl set id: 7e02ab0c-9bc2-4ffe-926c-5b388a07f7b2

Reported adverse events (FAERS/openFDA)#

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