Label: BIO-7 SERUM- nonapeptide-1, glutathione liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 71583-1002-1 - Packager: B.N.Trinity Co.,Ltd
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
DISCLAIMER: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.
Drug Label Information
Updated May 22, 2020
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- PURPOSE
- KEEP OUT OF REACH OF CHILDREN
- WARNINGS
- DOSAGE & ADMINISTRATION
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INACTIVE INGREDIENT
Chamomilla Recutita (Matricaria) Flower Water, Acetyl Hexapeptide-8, Palmitoyl Tripeptide-5, Palmitoyl Tetrapeptide-7, Palmitoyl Pentapeptide-4, Nonapeptide-1, Adenosine, Carnosine, Glutathione, Glycine Soja (Soybean) Phytoplacenta Extract, Hyaluronic Acid, Chrysanthemum,Indicum Flower Extract,Nelumbo Nucifera Extract, Rosa Multiflora Flower Extract,
HelichrysumArenarium Extract,SclerocaryaBirrea Seed Oil, Caprylic/Capric Triglyceride, Polyglyceryl-2 Laurate, Rosa Canina Fruit Oil,NelumbiumSpeciosum Flower Oil, Ceramide NP, Carbomer, Polyquaternium-51, Niacinamide,Dexpanthenol, Allantoin, 1,2-Hexanediol,
Caprylyl Glycol, Citrus Aurantium Amara (Bitter Orange) Flower Oil
- INDICATIONS & USAGE
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
BIO-7 SERUM
nonapeptide-1, glutathione liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:71583-1002 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength NONAPEPTIDE-1 (UNII: 64W45420K5) (NONAPEPTIDE-1 - UNII:64W45420K5) NONAPEPTIDE-1 5 g in 100 mL GLUTATHIONE (UNII: GAN16C9B8O) (GLUTATHIONE - UNII:GAN16C9B8O) GLUTATHIONE 3 g in 100 mL Inactive Ingredients Ingredient Name Strength CARNOSINE (UNII: 8HO6PVN24W) ADENOSINE (UNII: K72T3FS567) NIACINAMIDE (UNII: 25X51I8RD4) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:71583-1002-1 50 mL in 1 TUBE; Type 0: Not a Combination Product 05/22/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 05/22/2020 Labeler - B.N.Trinity Co.,Ltd (693708220) Registrant - B.N.Trinity Co.,Ltd (693708220) Establishment Name Address ID/FEI Business Operations B.N.Trinity Co.,Ltd 693708220 manufacture(71583-1002)