Label: NEUROTOX HAND NEURO- alcohol gel
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Contains inactivated NDC Code(s)
NDC Code(s): 76882-0002-1 - Packager: BIO-FD&C. Co., Ltd.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph not final
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.
Drug Label Information
Updated May 6, 2020
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- Official Label (Printer Friendly)
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PRINCIPAL DISPLAY PANEL
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.• 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 -
INGREDIENTS AND APPEARANCE
NEUROTOX HAND NEURO
alcohol gelProduct 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)