NDC | 71673-0004-1 |
Set ID | 5700e699-878c-03ed-e054-00144ff8d46c |
Category | HUMAN OTC DRUG LABEL |
Packager | MSCO |
Generic Name | |
Product Class | Adenosine Receptor Agonist |
Product Number | |
Application Number |
- ACTIVE INGREDIENT
-
INACTIVE INGREDIENT
Water
Glycerin
Butylene Glycol
Hydrogenated Polydecene
Cyclopentasiloxane
Cyclohexasiloxane
1,2-Hexanediol
Butyrospermum Parkii (Shea) Butter
Dimethicone
Polysorbate 60
Hydrogenated Polyisobutene
Jojoba Esters
Polyacrylate-13
Cetearyl Olivate
Sorbitan Olivate
Cetearyl Alcohol
Cetearyl Glucoside
Cetyl Alcohol
Glyceryl Stearate
Phytosteryl/Isostearyl/Cetyl/Stearyl/Behenyl Dimer Dilinoleate
Polyisobutene
Caprylyl Glycol
Phenoxyethanol
Sodium Polyacrylate
Dimethicone Crosspolymer
Fragrance(Parfum)
Polysorbate 20
Sorbitan Isostearate
Dipotassium Glycyrrhizate
Ethylhexylglycerin
Disodium EDTA
Hydroxypropyl Starch Phosphate
Coccinia Indica Fruit Extract
Eclipta Prostrata Extract
Dextrin
Theobroma Cacao (Cocoa) Extract
Propanediol
Euterpe Oleracea Fruit Extract
Hippophae Rhamnoides Fruit Extract
Rubus Idaeus (Raspberry) Fruit Extract
Dipeptide Diaminobutyroyl Benzylamide Diacetate
Tocopherol
Anemarrhena Asphodeloides Root Extract
Croton Lechleri Resin Extract
Combretum Farinosum Flower Nectar
Acetyl Hexapeptide-8 - PURPOSE
- KEEP OUT OF REACH OF CHILDREN
- INDICATIONS & USAGE
- WARNINGS
- DOSAGE & ADMINISTRATION
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
DPC NOBLESSE SUTA EYE
niacinamide, adenosine creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:71673-0004 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ADENOSINE (UNII: K72T3FS567) (ADENOSINE - UNII:K72T3FS567) ADENOSINE 0.04 g in 100 mL NIACINAMIDE (UNII: 25X51I8RD4) (NIACINAMIDE - UNII:25X51I8RD4) NIACINAMIDE 2 g in 100 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) GLYCERIN (UNII: PDC6A3C0OX) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:71673-0004-1 20 mL in 1 TUBE; Type 1: Convenience Kit of Co-Package 07/01/2017 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 07/01/2017 Labeler - MSCO (689039838) Registrant - MSCO (689039838) Establishment Name Address ID/FEI Business Operations MSCO 689039838 label(71673-0004) Establishment Name Address ID/FEI Business Operations Cosmax, Inc 689049693 manufacture(71673-0004)