NEUROTOX HAND NEURO- alcohol gel

NEUROTOX HAND NEURO by

Drug Labeling and Warnings

NEUROTOX HAND NEURO by is a Otc medication manufactured, distributed, or labeled by BIO-FD&C. Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

PRINCIPAL DISPLAY PANEL

Antiseptic

Alcohol

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

For the external use only

. 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

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.

Keep out of reach of children

INGREDIENTS AND APPEARANCE

NEUROTOX HAND NEURO 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 76882-0002
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	37.2 mL  in 60 mL

Inactive Ingredients
Ingredient Name	Strength
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
WATER (UNII: 059QF0KO0R)
1,2-HEXANEDIOL (UNII: TR046Y3K1G)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 76882-0002-1	60 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	05/01/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	05/01/2020

Labeler - BIO-FD&C. Co., Ltd. (688203268)

Registrant - BIO-FD&C. Co., Ltd. (688203268)

Establishment
Name	Address	ID/FEI	Business Operations
BIO-FD&C. Co., Ltd.		688203268	manufacture(76882-0002)