NEUROTOX HAND NEURO- alcohol gel 
BIO-FD&C. Co., Ltd.

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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1

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

NEUROTOX HAND NEURO 
alcohol gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:76882-0002
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL37.2 mL  in 60 mL
Inactive Ingredients
Ingredient NameStrength
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)  
WATER (UNII: 059QF0KO0R)  
1,2-HEXANEDIOL (UNII: TR046Y3K1G)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:76882-0002-160 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product05/01/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A05/01/2020
Labeler - BIO-FD&C. Co., Ltd. (688203268)
Registrant - BIO-FD&C. Co., Ltd. (688203268)
Establishment
NameAddressID/FEIBusiness Operations
BIO-FD&C. Co., Ltd.688203268manufacture(76882-0002)

Revised: 5/2020
Document Id: a4f488fd-4e69-bdfb-e053-2a95a90a0db7
Set id: a4f48769-e470-1004-e053-2995a90af319
Version: 1
Effective Time: 20200506
 
BIO-FD&C. Co., Ltd.