Label: STOP-AGING PEPTIDE EYE- niacinamide, adenosine cream
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Contains inactivated NDC Code(s)
NDC Code(s): 74997-0004-1 - Packager: J&J COMPANY
- Category: HUMAN OTC DRUG LABEL
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 August 10, 2020
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
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INACTIVE INGREDIENT
Water, Butylene Glycol, Glycerin, Caprylic/Capric Triglyceride, Butylene Glycol Dicaprylate/Dicaprate, Niacinamide, Beeswax, Coco-Caprylate/Caprate, Cetearyl Alcohol, Cetearyl Olivate, Behenyl Alcohol, Glyceryl Stearate, Trehalose, Sorbitan Olivate, Sodium Acrylate/Sodium Acryloyldimethyl Taurate Copolymer, Arginine, Carbomer, Polyisobutene, Cetearyl Glucoside, Xanthan Gum, Arachidyl Alcohol, Stearyl Alcohol, Hydrogenated Olive Oil Unsaponifiables, Adenosine, Caprylyl/Capryl Glucoside, Sorbitan Oleate, Glucose, Hydrogenated Polyisobutene, Centella Asiatica Extract, Hyaluronic Acid, Palmitoyl Tripeptide-5, Pentylene Glycol, Caprylyl Glycol, Anemarrhena Asphodeloides Root Extract, Disodium EDTA, Glyceryl Caprylate, Chlorphenesin, 1,2-Hexanediol
- 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 EYE
niacinamide, adenosine creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:74997-0004 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:74997-0004-1 30 mL in 1 TUBE; 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(74997-0004) , label(74997-0004) , pack(74997-0004)