Label: STOP-AGING PEPTIDE TONER- niacinamide, adenosine liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 74997-0007-1 - Packager: J&J COMPANY
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
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Drug Label Information
Updated October 7, 2020
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
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INACTIVE INGREDIENT
Water, Butylene Glycol, Glycerin, Niacinamide, PEG/PPG-17/6 Copolymer, PEG-60 Hydrogenated Castor Oil, 1,2-Hexanediol, Caprylyl Glycol, Aloe Barbadensis Leaf Extract, Centella Asiatica Extract, Allantoin, Carbomer, Tromethamine, Adenosine, Ethylhexylglycerin, Dipotassium Glycyrrhizate, Lavandula Angustifolia (Lavender), Flower Extract, Rosmarinus Officinalis (Rosemary), Leaf Extract, Origanum Vulgare Extract, Thymus Vulgaris (Thyme), Flower/Leaf/Stem Extract, Pentylene Glycol, Aspalathus Linearis Extract, Glycyrrhiza Glabra (Licorice) Root Extract, Hydrogenated Polyisobutene, Commiphora Myrrha Resin Extract, Perilla Frutescens Leaf Extract, Yucca Schidigera Root Extract, Nicotinoyl Tripeptide-1,Palmitoyl pentapeptide-4, Caffeoyl sh-Octapeptide-4, Caffeoyl Tripeptide-1, sh-Octapeptide-4, sh-Decapeptide-9, sh-Pentaptpdie-19, Anemarrhena Asphodeloides Root Extract, Fragrance (Butylphenyl Methylpropional, Linalool)
- PURPOSE
- KEEP OUT OF REACH OF CHILDREN
- INDICATIONS & USAGE
- WARNINGS
- DOSAGE & ADMINISTRATION
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
STOP-AGING PEPTIDE TONER
niacinamide, adenosine liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:74997-0007 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength NIACINAMIDE (UNII: 25X51I8RD4) (NIACINAMIDE - UNII:25X51I8RD4) NIACINAMIDE 2 g in 100 mL ADENOSINE (UNII: K72T3FS567) (ADENOSINE - UNII:K72T3FS567) ADENOSINE 0.04 g in 100 mL Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:74997-0007-1 250 mL in 1 BOTTLE; Type 0: Not a Combination Product 08/10/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 08/10/2020 Labeler - J&J COMPANY (688995236) Registrant - J&J COMPANY (688995236) Establishment Name Address ID/FEI Business Operations J&J COMPANY 688995236 manufacture(74997-0007) , label(74997-0007) , pack(74997-0007)