FDA.reportPublic FDA data

NEUROTOX HAND NEURO

Manufacturer
BIO-FD&C. Co., Ltd.
Effective date
2020-05-06
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:09:51

Label at a glance#

ProductNEUROTOX HAND NEURO
Active ingredientALCOHOL
Label structure1 sections

Label contents#

Full prescribing information#

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

11

OTC - PURPOSE SECTION

Antiseptic

OTC - ACTIVE INGREDIENT SECTION

Alcohol

INACTIVE INGREDIENT SECTION

Water, Ferulic Acid, Gallic Acid, sh Decapeptide 7, sh Octapeptide 4, sh Oligopeptide
9, sh Pentapeptide 19, Diospyros Kaki Leaf Extract, Vitis Vinifera (Grape) Fruit Extract, Coffea Arabica (Coffee) Seed Extract, Carthamus Tinctorius (Safflower) Flower Extract, Polygonum Cuspidatum Root Extract, Camellia Sinensis Leaf Extract, Castanea Crenata (Chestnut) Shell Extract, Zanthoxylum Piperitum Fruit Extract, Butylene Glycol, Carbomer, Tromethamine, 1,2 Hexanediol, Fragrance

DOSAGE & ADMINISTRATION SECTION

For the external use only

WARNINGS SECTION

.• Flammable. Keep away from fire or flame.
• For external use only.
• When using this product do not use in or near the eyes.
In case of contact, rinse eyes thoroughly with water.
• Stop use and ask a doctor if irritation or rash appears
and lasts.
• Keep Out of Reach of Children.
• Do not eat.
• If swallowed, get medical help or contact a Poison Control
Center right away

INDICATIONS & USAGE SECTION

Directions
• Put enough product in your palm to cover hands and rub
hands together briskly until dry.
• Children under 6 years of age should be supervised when
using. Not recommended for infants.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
581660ethanol 62 % Topical GelPSN1
581660ethanol 0.62 ML/ML Topical GelSCD1
581660ethanol 62 % Topical GelSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
76882-0002-12023-01-30C16284748780-1f386c64a-45a8-0266-e053-dadaa90a7c1aa4f48769-e470-1004-e053-2995a90af319

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
76882-0002-1NEUROTOX HAND NEURO60 mL in 1 BOTTLE, PUMPGEL601

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
76882-0002NEUROTOX HAND NEURO (ALCOHOL) GEL [BIO-FD&C. CO., LTD.]1Legacy NDC, 1 package rows20200506_a4f48769-e470-1004-e053-2995a90af319.zip

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
76882-000276882-0002-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Name, UNII, Kind table
NameUNIIKind
BUTYLENE GLYCOL3XUS85K0RAIACT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE0A5MM307FCIACT
WATER059QF0KO0RIACT
1,2-HEXANEDIOLTR046Y3K1GIACT
ALCOHOL3K9958V90MACTIB

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
a4f488fd-4e69-bdfb-e053-2a95a90a0db7a4f48769-e470-1004-e053-2995a90af3192020-05-06WarningsExact identifier
spl id: a4f488fd-4e69-bdfb-e053-2a95a90a0db7
spl set id: a4f48769-e470-1004-e053-2995a90af319

Reported adverse events (FAERS/openFDA)#

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