NDC | 71551-0001-1 |
Set ID | 52fb9365-5c1a-264a-e054-00144ff88e88 |
Category | HUMAN OTC DRUG LABEL |
Packager | G&J Co., Ltd. |
Generic Name | |
Product Class | Adenosine Receptor Agonist |
Product Number | |
Application Number |
- ACTIVE INGREDIENT
-
INACTIVE INGREDIENT
WATER, GLYCERIN, DIPROPYLENE GLYCOL, DIMETHICONE, CAPRYLIC/CAPRIC TRIGLYCERIDE, HYDROGENATED POLY(C6-14 OLEFIN), GLYCERETH-26, BUTYROSPERMUM PARKII (SHEA) BUTTER, POLYGLYCERYL-10 STEARATE, POLYGLYCERYL-3 METHYLGLUCOSE DISTEARATE, BIFIDA FERMENT LYSATE, BUTYLENE GLYCOL, DIOSCOREA JAPONICA ROOT EXTRACT, C12-15 ALKYL BENZOATE, NEOPENTYL GLYCOL DIHEPTANOATE, PENTAERYTHRITYL DISTEARATE, SACCHAROMYCES FERMENT FILTRATE, PIPER METHYSTICUM LEAF/ROOT/STEM EXTRACT, ROYAL JELLY EXTRACT, SALVIA MILTIORRHIZA ROOT EXTRACT, ROSA CENTIFOLIA FLOWER WATER, HYDROGENATED LECITHIN, ARGANIA SPINOSA KERNEL OIL, 1,2-HEXANEDIOL, POLYSORBATE 20, TRANEXAMIC ACID, AMMONIUM ACRYLOYLDIMETHYLTAURATE/VP COPOLYMER, ACRYLATES/C10-30 ALKYL ACRYLATE CROSSPOLYMER, TROMETHAMINE, GLUTATHIONE, ETHYLHEXYLGLYCERIN, XANTHAN GUM, POLYQUATERNIUM-51, GLYCOSYL TREHALOSE, SORBITAN LAURATE, HYDROGENATED STARCH HYDROLYSATE, RAFFINOSE, BIOSACCHARIDE GUM-1, GLYCERYL POLYMETHACRYLATE, DISODIUM EDTA, LECITHIN, BISABOLOL, CARBOMER, HYDROXYETHYLCELLULOSE, ACETYL DIPEPTIDE-1 CETYL ESTER, INOSITOL, PANTHENOL, DICAPRYLYL CARBONATE, SODIUM POLYACRYLATE, SUCROSE DISTEARATE, CERAMIDE NP, FOLIC ACID, ACETIC ACID, CHOLESTEROL, LACTIC ACID, PALMITOYL PENTAPEPTIDE-4, FRAGRANCE, PHENOXYETHANOL, POTASSIUM SORBATE
- PURPOSE
- KEEP OUT OF REACH OF CHILDREN
- INDICATIONS & USAGE
-
WARNINGS
•Precautions when using1. After using or using cosmetics, consult a specialist if you have any abnormal symptoms such as red spots, swelling or itching or side effects caused by direct sunlight.
2. Do not use on wounded area
3. storage and handling Precautions
a) Keep out of the reach of children
b) Store away from direct sunlight.
- DOSAGE & ADMINISTRATION
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
SOLLUME ESTHE REPAIR SERUM
niacinamide, adenosine gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:71551-0001 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 5 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:71551-0001-1 4 in 1 PACKAGE 05/01/2017 1 7.5 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 05/01/2017 Labeler - G&J Co., Ltd. (694841570) Registrant - G&J Co., Ltd. (694841570) Establishment Name Address ID/FEI Business Operations Kolmar Korea Co., Ltd. 689512611 manufacture(71551-0001) Establishment Name Address ID/FEI Business Operations G&J Co., Ltd. 694841570 label(71551-0001)