Neurotox Hand Neuro
Product Images NDC 76882-0002

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This gallery contains 1 technical images submitted to the FDA as part of the official labeling for Neurotox Hand Neuro (NDC 76882-0002). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Bio-fd&c. Co., Ltd., these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

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FDA Label Image

1 (02label Neurotoxhandneurogel)

1 (02label Neurotoxhandneurogel)
NEUROTOX HAND NEURO GEL is a hand sanitizer to help reduce bacteria on the skin. It contains alcohol (62%), water, Ferulic Acid, Gallic Acid, sh-Decapeptide-7, sh-Octapeptide, 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, and Fragrance. It is flammable and should be kept away from fire or flame. Keep out of reach of children and do not eat. If swallowed, get medical help or contact a Poison Control Center right away. Not recommended for infants. The product should be used externally and should not be used in or near the eyes. If the product causes irritation or rash, stop using it and consult a doctor. It comes in a bottle weighing 60 ml or 2.02 fl oz. The manufacturer is BIO-FD&C Co., Ltd, located in Korea.*

* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.